• Analytical Science and Technology
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• v.7 no.3
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• pp.271-276
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• 1994

A Na-cellulose adsorbent was prepared by treating Sigma S-5504 cellulose with 2M NaOH and examined the adsorption behavior between metal ions and Na-cellulose in aqueous solution with batch method. Considering ion exchange capacity of Na-cellulose, the adsorption ratio of the Na-cellulose to metals charge equivalent indicated that the adsorption result from ion exchanging between metal ions and Na-cellulose. The enthalpy for the metal adsorption on the Na-cellulose was calculated to -18kcal/mol, which value was compared to those of carboxymethylcellulose(CMC) and Dowex 50W-X8, these result suggested that the adsorption on Na-cellulose resulted from ion exchange adsorption.

• Journal of the Korean Chemical Society
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• v.38 no.2
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• pp.122-128
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• 1994

Macrocyclic ligand has been known to selectively bind with metal ions so that ability applied for the transport of metal ions across the emulsion liquid membrane in this study. The metal ions are transproted from the source phase to the receiving phase by the carrier of the organic phase. Several factors involved in the transport of metal ions acrose the emulsion membrane we reported here and these factors provided the informations for the selective seperation of some metal ion. Stability constants for cation-macrocyclic ligand and metal ion-anion receiving phase interaction are examined as parameters for the prediction of metal ion transport selectivities. $Pb^{2+}$ was transported higher rates than the other metal ions in the mixture solution. The interaction of metal ion to anion in receiving phase is important. $S_2O_3^{2-}$- in replacement of $NO_3^-$ in the receiving phase enhances the transport of $Pb^{2-}$since $Pb^{2-}-S_2O_3^{2-}$interaction is greater than $Pb^{2+}-NO_3^-$ interaction.

• Journal of the Institute of Electronics Engineers of Korea TE
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• v.37 no.2
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• pp.1-5
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• 2000

We have investigated dielectric properties of IMI-O LB films for the effect of complex concentration by electrical conductivity, dielectric constant and dielectric relaxation time at different frequencies. In the surface pressure-area$\pi$-A) isotherms for the increase of $FE^{3+}$ concentration, the molecular area was expanded with $FE^{3+}$concentration increase by electrostatic repulsion between the polymer chains and hydrophobic increase of ionic strength. In the I-V characteristics, it is found that the limiting area has effects on the change of conductivity And, the dielectric relaxation time decreased for increase of the $FE^{3+}$concentration.

• Journal of the Korean Chemical Society
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• v.38 no.2
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• pp.129-135
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• 1994

Acyclic polyether dicarboxylic acid have been studied as metal cation carriers in a bulk liquid membrane system. The proton-ionizable ligands feature allows the coupling of a cation transport to reverse proton transport. This feature offers promise for the effective separation and concentration of metal cations with the metal cation transport being driven by a pH gradient. Metal cation transport increased regularly with increasing hydroxide($H^-$) concentration of source phase and with proton($H^+$) concentration of receiving phase. Competitive transport by the acyclic polyether dicarboxylic acids is selective for calcium ion over other alkaline-earth cations.

• KSBB Journal
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• v.8 no.4
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• pp.370-374
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• 1993

In transportation the amount of metal ion by crown ethers, dibenzo-18-crown-6 were investigated using ultraviolet spectrometer. Transported the amount of one valence metal ion as $K^+ and Li^+}$ was not so much. On the other hand, two valence metal ion increased by dibenzo-18-crown-6, which means that the ionic charge and hydration of two valence metal ion affected the carrying ability of crown ethers. The carrying ability of dibenzo-18-crown-6 was, therefore, adequate for two valence metal ion as $Ca^{2+}$ and $Ba^{2+}$. It was also suggested that transport metal ion by crown ethers, which is related rather the catching ability than the selectivity of metalion.

• Proceedings of the Korean Vacuum Society Conference
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• 2011.02a
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• pp.463-463
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• 2011

집속이온빔장치(Foucused Ion Beam)에서 사용하는 액체금속이온원(Liquid Metal Ion Source)은 고 전류밀도, 고 휘도, 낮은 에너지퍼짐 등 많은 장점이 있다. 대부분의 집속이온빔 장치에서 플라즈마 이온소스에 비해 빔의 직경이 작고 GFIS 보다 다루기 쉬워 액체금속이온원을 많이 사용하고 있다. 기존에 사용하던 액체금속이온원에 서프레셔라는 새로운 전극을 추가시켜 팁과 갈륨저장소, 서프레셔, 추출극 구조로 만들었다. 이 연구를 위해 RPA(Retarding Potential Analyser)를 제작 하였다. RPA는 두 개의 메쉬와 하나의 컬렉터로 이루어져 있으며, 액체금속이온과 플로팅 되어있는 RPA에 전압의 차이를 주기위해 베터리로 제작한 파워로 액체금속이온에 인가되는 전압에 + 90V, -90V까지 제어가 가능하게 만들었다. 본 연구에서는 서프레셔의 유무에 따른 액체금속이온원의 에너지 퍼짐에 대해 연구하였다. 추출극에 전압 변화를 주어 방출되는 전류를 5uA, 10uA, 15uA, 20uA로 변화시켜가며 RPA에서 측정되는 전류를 가지고 전류-전압의 관계를 보았고, 에너지 퍼짐정도를 알았다. 마찬가지로 서프레셔에 전압 변화를 주어 전류-전압 관계, 에너지 퍼짐정도를 알았다.

• Proceedings of the Membrane Society of Korea Conference
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• 1998.10a
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• pp.130-132
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• 1998

정밀여과막(MF)막은 $0.1~1\mum$정도의 공경을 가지고 있는 막으로 산업이나 생활분야에서 널리 사용되고 있다. 이러한 정밀여과막에 이온교환기를 부여 시키므로써, 필요로하는 금속이온이나 단백질을 흡착할 수 있는 기능성 분리막이 제조 가능하다. 방사선프라프트 중합법은 고분자를 개질, 수식 또는 기능화시키는 수법으로 사용되고 있다. 본 실험에서는 방사선그라프트중합법을 사용하여 폴리에틸렌 정밀여과막에 에폭시기를 가지는 glycidyl methacrylate(GMA)를 그라프트 중합시킨 후 이온 교환기를 도입하여, 얻어진 막의 특성에 대해 고찰하였다. 본실험의 목적은 다음과 같다. (1) 폴리에틸렌 정밀여과 막에 방사선그라프트 중합법을 사용하여 이온교환기를 도입시키는 반응조건을 검토한다. (2) 도입된 이온교환기에 다른 막의 투과 성능을 조사한다. (3) 투과법에 의한 금속이온의 흡착성능을 조사한다. 여기서, 이온교환기로서는 술폰산(sodium sulfite:$SO_3H$)을 사용하였다.

• Journal of Life Science
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• v.12 no.6
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• pp.682-687
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• 2002

We analyzed improvement on the enzyme activity of CPase Taq by addition of various metal ions. The enzyme activity was increased more then four times by 1 mM cobalt ion and almost three times by 1 mM calcium ion. However, the active center metal zinc ion did not affect the enzyme activity. In order to investigate whether the active center metal affects the enzyme activity, zinc ion which is occupied the active center of the enzyme was replaced by cobalt ion which activates the enzyme activity very effectively. Since the cobalt ion in the active center of the cobalt-substituted CPase Taq did not affect the enzyme activity, it could act as the natal metal ion in the active center of the enzyme.

• Journal of the Korean Chemical Society
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• v.29 no.4
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• pp.341-347
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• 1985

Formation of metal complex is the first step in the many biological actions of metal ions present in the biological systems. In this work the not electron affinity necessary for the formation of such metal complexes has been determined for a series of metal ions. It has been found that excess polarizing strength can be adopted as a measure of electron affinity and trend is the excess polarizing strength is related to Irving-Williams series. Those metal ions having greater than 0.22 in value of excess polarizing strength have been found to show carcinogenicity and other metal ions, which are supposed to be carcinogenic, have shows to have greater than 0. 22 in value of excess polarizing strength, demonstrating that excess polarizing strength could be used to determine if any metal ion possesses carcinogenic activity.

• Economic and Environmental Geology
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• v.45 no.2
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• pp.205-215
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• 2012

Metal ions, toxic or potentially toxic to biota and human beings, can be immobilized by sorption onto the mineral surfaces in soils and sediments. This article briefly explains theories regarding the chemical properties of mineral surfaces to sorb metal ions and processes of extended X-ray absorption fine structure (EXAFS) analysis for sorption study, and reviews atomic-scale findings on metal sorption on mineral surfaces. The theoretical understanding on the chemistry of mineral surfaces and metal sorption is fundamental to the proper analysis of the atomic-scale spectroscopy to determine the sorption phases. Atomic-scale findings on metal sorption phases discussed here include co-precipitation, ternary complexation, aging effects, and desorption possibilities, as well as outer-sphere complexation, inner-sphere complexation, and surface precipitation.