• Journal of the Korean Chemical Society
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• v.36 no.6
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• pp.791-795
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• 1992

The limiting equivalent conductances of LiCl, NaCl, KCl and KBr have been obtained in water using conductometric method from 1 to 2000 bars at $25^{\circ}C$. From the limiting equivalent ionic conductances (obtained using TATB[Tetraphenyl Arsonium Tetraphenyl Borate]method) of $Li^+$, $Na^+$, $K^+$, $Cl^-$, and $Br^-$ ions and viscosity of water at given pressure, their Stokes radii have been calculated. From the corrected radii caliberated by Nightingale method and the crystallographic radii at a given pressure, the volume of hydration-shell surrounding ion was calculated and hydration numbers of $Li^+$, $Na^+$, $K^+$, $Cl^-$, and $Br^-$ ions were obtained. From the experimental results, it was found that the hydration number of $Li^+$, $Na^+$, $K^+$, $Cl^-$, and $Br^-$ ions slightly decreased with increasing pressure. This trend may be explained by Horne's suggestion[Advances in High Pressure Research]. Comparing results of this study with those of Nakahara's, the hydration numbers of $K^+$ and $Cl^-$ ions were almost twice as large as those of Nakahara's[Rev. Phys. Chem. Japan, 42, 12 (1972)]. By comparing the present results with those of Kollman's [J. Am. Chem. Soc., 113, 2481 (1991)], the hydration number obtained by applying TATB method and Nightingale method may be inferred to be reasonable.

• Journal of the Korean Chemical Society
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• v.33 no.2
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• pp.164-167
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• 1989

The rate for the aquation of $trans-[Cr(tmd)_2FX]^+(X=F^-,\;Cl^-)$ ion in aqueous acidic solution has been measured by spectrophotometric method at various temperatures and pressures. The rate constants are increased with increasing temperatures and pressures. The values of activation entropy are 5.2 eu for $trans-[Cr(tmd)_2F_2]^+$ and -16.62 eu for $trans-[Cr(tmd)_2FCl]^+$ ions. Activation volumes have all negative values and lie in the limited range $-3∼-2\;cm^3mol^{-1}$ for $trans-[Cr(tmd)_2F_2]^+$ and $-8∼-7\;cm^3mol^{-1} for $trans-[Cr(tmd)_2FCl]^+$ ion. From the above results, we may deduce that the mechanism for the aquation of $trans-[Cr(tmd)_2F_2]^+$ and $trans-[Cr(tmd)_2FCl]^+$ ions is interchange-associative mechanism and dissociative mechanism respectively.

• Journal of the Korea Concrete Institute
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• v.27 no.1
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• pp.85-92
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• 2015

The chloride ions, responsible for the initiation of the corrosion mechanism, intrude from the external medium into the concrete. A part of the intruding chloride ions will be retained by the hydration products of the binder in concrete, either through chemical adsorption or by physical adsorption. Since the hydration products of cement are responsible for the chloride binding in concrete, this study focused on the chloride binding in individual hydrate. The purpose of this study is to explore the time dependant behaviors of chloride ions adsorption with cement hydrates, focused on its mechanism. AFt phase and CH phase were not able to absorb chloride ion, however, C-S-H phase and AFm phase had a significant chloride adsorption capacity. In particular, AFm phase showed a chemical adsorption with slow rate in 40 days, while C-S-H phase showed binding behaviors with 3 stages including momentary physical adsorption, physico-chemical adsorption, and chemical adsorption. Based on the results, this study suggested theoretical approach to depict chloride adsorption behavior with elapsed time of C-S-H phase and AFm phase effectively. It is believed that the approach suggested in this study can provide us with a good solution to understand the mechanism on chloride adsorption with hydrates and to calculate a rate of chloride penetration with original source of chloride ions, for example, marine sand at initial time or sea water penetration later on.

• Journal of the Korean Chemical Society
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• v.20 no.6
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• pp.448-452
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• 1976

A simplified statistical mechanical method was developed for the calculation of the dehydration fraction, activation free energy of dehydration, and the relaxation times of hydrated ions. The model used includes the equilibrium constant between hydrated and dehydrated water, a water-ion interaction potential energy term, and a mixing factor for the species present. The agreement between theory and experiment is good. The pressure dependence of ion dehydration is also discussed.

• The Korean Journal of Pesticide Science
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• v.6 no.3
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• pp.175-182
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• 2002

This experiment was conducted to investigate the effects of acid rain in spraying copper hydroxide 77% wettable power(WP) on leaf surface morphology and crop injury of the garlic(Allium sativum L.). Leaf chlorosis, hooked leaves, wrinkled epidermal cells and increased stomata open of garlic were induced by foliar application of simulated acid rain(SAR). It was become to be severe in application of copper hydroxide solution after application of SAR, but those yield of garlic was not significantly different from the untreated control. Leaf chlorosis was sharply increased above 100 ppm of copper ions. Amount of solved copper ions in copper hydroxide solution was remarkably increased below pH 5.5 and the residue in garlic leaves was significantly increased by application of copper hydroxide solution after spraying SAR compared with application of copper hydroxide solution only. When calcium carbonate was applied together with copper hydroxide leaf chlorosis was less than copper hydroxide only.

• Resources Recycling
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• v.27 no.2
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• pp.63-67
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• 2018

Gibbs free energy is a measure of relative stability among substances. Since the nature of the ions in aqueous solution is diverse, their thermodynamic data at extensive experimental conditions is scarce. In this work, the calculation procedure was introduced to obtain the absolute and conventional standard molar enthalpies and entropies of hydration of ions from the standard enthalpies and entropies of formation of hydrated ions. The application of correspondence principle to estimate thermodynamic data at high temperature was explained.

• Proceedings of the KAIS Fall Conference
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• 2002.05a
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• pp.137-139
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• 2002

이온교환은 액체상 이온과 고체상 이온간의 화학반응이며 연수 및 탈염공정, 특정물질의 제거 및 회수, 토양을 통한 이온성 물질의 이동에서 널리 이용되고 있다. 이온교환수지는 이온교환시 원자가가 높을수록, 수화반경이 작을수록, 이온농도가 낮을수록 증가한다. 본 연구는 이온교환수지에 대한 평형실험을 선택도가 칼럼실험에 적용되는지 조사하였다. 이 실험치 결과에서 음이온 교환수지의 선택도 순서는 OH/sup -/ < F/sup -/ < HCO₃/sup -/ < Cl/sup -/ < Br/sup -/ ≤ No₃/sup -/ < So₄/sup 2-/ 이였으며, 음이온 칼럼 교환도 동일하였다. 또한 바탕 양이온의 가수가 높을수록 이온교환이 빠르게 진행됨을 알 수 있다.

• Journal of the Korean Ceramic Society
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• v.36 no.3
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• pp.260-265
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• 1999

보통 포틀랜드 시멘트와 플라이애쉬, 슬래그를 혼합한 혼합시멘트 경화체를 이용하여 이온 확산에 미치는 혼합재의 영향과 양이온 공존시 염소이온의 확산에 대하여 고찰하였다. 겉보기 이온확산계수가 보통 포틀랜드의 시멘트보다 플라이애쉬와 슬래그를 혼합한 시멘트 경화체가 약 10-3배로 매우 낮은 값을 나타내었다. 이것은 포졸란 반응에 의해 많은 CSH 수화물이 capillary pore에 형성되어 macro pore가 감소되고 micro pore가 증가되어 이온 확산에 대한 저항이 커졌기 때문이다. 또한, Mg2+이온 공존시에 염소이온의 확산은 증가되었다.

• Journal of the Korean Ceramic Society
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• v.34 no.2
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• pp.163-170
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• 1997

The retarding effects of MgSiF6.6H2O on the hydration of portland cement were studied. The setting time, flow value and compressive strength of mortar were measured and the mechanism of retardation was also studied by ion concentration in solution, SEM, BET, and X-ray diffraction. The results are as follows ; 1. Setting time was delayed by the addition of MgSiF6.6H2O. 2. The flow value of mortar decreases depending upon the amount of MgSiF6.6H2O. 3. The compressive strength was almost same or some increase on 28 days hydration. 4. The main retardation mechanism of MgSiF6 on the hydration of portland cement may be explained by the following hypothesis. MgSiF6 depressing the Ca++ and K+ ion concentration of cement paste solution be-cause of the recrystalization of K2SiF6 and CaF2 phase. The new products of K2SiF6 and CaF2 deposit on the surface of unhydrated cement powder and harzard the mass transfer through these layer. The low con-centration of Ca++, K+ ion in solution was decreasing the hydration rate of portland cement.

• Proceedings of the KAIS Fall Conference
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• 2003.06a
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• pp.322-324
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• 2003

이온교환은 액체상에 존재하는 이온과 고체상에 존재하는 이온이 당량적으로 치환되는 것으로 정의하며, 치환되는 정도는 일반적으로 전하의 크기와 이온이 수화반경에 따라 달라진다. 지금까지의 이온교환 반응에 대한 모델링 연구는 실험식, 질량작용식, 열역학식, 전기이중층이론, 표면착화모델 등을 이용하여 2 성분에 대하여 다양한 시도를 하였다. 본 연구에서는 2, 3, 4성분에 대해 질량작용법칙과 전기이중층이론을 조합한 표면착화모델과 질량작용법칙을 이용한 모델을 수행하였다. 그 결과 표면착화모델이 질량작용법칙을 이용한 것보다 실험치와 일치함을 알 수 있었다.