• Proceedings of the Optical Society of Korea Conference
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• 2000.02a
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• pp.262-263
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• 2000

이온교환방법은 착색된 유리를 생산하기 위하여 수세기 전부터 연구되어 왔다. 1972년 Izawa와 Nagome가 silicate 유리에 Tl$^{+}$이온을 치환하여 평판 도파로를 만든 후, 이온교환은 도파로나 마이크로 렌즈제작 등에 활발하게 연구되어 왔다. 유리 도파로는 광의 진행손실이 적으며, 광섬유와의 우수한 호환성, 그리고, 제작이 용이하고 가격이 싼 장점 등으로 인하여 많은 연구가 진행되고 있는 재료이다. 그러나, 유리에 이온교환으로 광소자를 만들기 위해서는 굴절률변화를 정확하게 예측해야한다. 따라서, 유리에서 이온들의 확산특성을 정확하게 분석하고 실험적으로 확립하는 연구는 매우 중요하다고 하겠다. (중략)

• 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 Electrochemical Society
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• v.9 no.3
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• pp.132-134
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• 2006

The main component governing selectivity in ion-selective electrodes and optodes is the ionophore. For this reason, a member of natural products that possess selective ion-binding properties have long been sought after. By applying this principle, the performance of tetracycline used as neutral carriers for cation selective polymeric membrane electrode was investigated. The cation ion-selective electrode based on tetracycline gave a good Nernstian response of 26.6 mV per decade for calcium ion in the activity range $1x10^{-6}M$ to $1x10^{-2}M$ with and without lipophilic additives. The optimized cation ion-selective membrane electrodes displayed very comparable potentiometric responses to various mono and di-valent cations of alkali and alkaline earth metal ions except $Mg^{2+}$.

• Membrane Journal
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• v.31 no.1
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• pp.1-15
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• 2021

The membrane-based CO2 capture is a fast-growing branch in gas separating field. Ionic liquid assisted mixed matrix membrane (MMM), which consists of organic fillers with dispersed ionic liquid, shows high potentiality as a candidate for CO2 separation medium. In MMM, various kinds of ionic liquid and inorganic filler are incorporated into polymer to enhance gas separating performance. Especially, the strong interaction between ionic liquid and organic filler gives huge influence on enhancing the separating performance by increasing affinity, selectivity and adsorption of CO2 into the framework. Also the mechanical properties of metal organic framework are positively tuned by input of ionic liquid to improve CO2 permeability and selectivity. In this review, study of various combinations of ionic liquid and metal organic framework (MOF) in the polymeric membrane for carbon dioxide separation is discussed.

• Proceedings of the Membrane Society of Korea Conference
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• 1993.10a
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• pp.61-62
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• 1993

고분자 분리막의 투과성과 선택성을 향상시키기 위하여 IPN막, 고분자/액정 복합막을 다양한 기능을 가진 재료가 개발되고 있다. 본 연구에서는 알칼리메탈이온을 분리하기 위하여 고분자 지지체에 운반체로써 crown ether(macro-cyclic polyether)류를 분산시킨 고분자/운반체 복합박막을 제조하였다. 고분자/운반체 복합박막은 고분자와 운반체의 혼합용액을 수면에 전개시켜 제조하였다. 고분자는 PVC(M.W 60000, Aldrich), PS(M.W 280000, Aldrich)와 CA(M.W 30000, Sigma)를 사용하였고, 운반체로는 crown ether 중 $K^+$이온과 선택성을 가지는 18-Crown-6(Sigma)를 사용, 고분자와 18-Crown-6의 증량분을 달리하는 혼합용액을 제조하였다. 이때 용매는 Tetrahydrofuran를 사용하였다. 수면에 생성된 박막을 다공성 지지막에 적층시킨 후 감압 건조시켜 복합막을 제조하였다. 고분자와 운반체가 혼합되어 있는 용액의 점도와 표면장력을 각각 fluid spectrometer와 tensionmeter를 사용, 용액이 수면위에서 완전한 막을 형성하면서 분산될 수 있는지 조사하였으며, 고분자 지지체에 분산 고정된 운반체의 분산형태와 표면농도를 조사하기 위하여 ESCA를 이용하였다.

• Journal of the Korean Electrochemical Society
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• v.12 no.1
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• pp.40-46
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• 2009

We present a method for spatially selective immobilization of functional materials, such as proteins and nanoparticles, onto pre-activated silicon surfaces by electrochemical reaction. Carboxymethylbenzendiazonium (CMBD) cations, being adsorbable on silicon surfaces through electrochemically reductive deposition, is used as an anchor molecule to prepare the pre-activated silicon surfaces. It is demonstrated that the use of BD reaction is very efficient for the selective immobilization because the functional materials are immobilized exclusively onto the pre-adsorbed CMBD region. The method is applied to immobilize gold nanoparticles on the selected nanowire of the nanowire array.

• Korean Chemical Engineering Research
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• v.51 no.5
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• pp.615-621
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• 2013

Membrane characterization methods for aqueous redox flow batteries aqueous RFBs were modified for non-aqueous RFBs. The modified characterization methods, such as ion exchange capacity, transport number, permeability and single cell test, were carried out to evaluate commercial membranes in non-aqueous electrolyte. It was found that columbic efficiency and energy efficiency in a single cell test were dependent on the ion selectivity of commercial anion exchange membranes. Neosepta AHA anion exchange membrane showed the anion transport number of 0.81, which is a relatively low ion selectivity in non-aqueous electrolyte, however, exhibited 92% of coulombic efficiency and 86% of energy efficiency in a single cell test. It was also found that a porous membrane without ion selectivity is suitable for a non-aqueous redox flow battery at a high current density.

• Journal of the Korean Chemical Society
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• v.42 no.5
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• pp.531-538
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• 1998

The ion selective membrane electrode made of calix[4]arene-based host 1 as ionophore, poly (vinyl chloride) (PVC) as matrix and dioctylsebacate (DOS) as a plasticizer was studied. The potential responses of this membrane electrode to alkali, alkaline earth and transition metal cations were investigated. Especially this membrane electrode was turned out to be affinitive for $Pb^{2+}$ in the deionized water. It was observed that the response was linear in the concentration range from $1.0 \times 10^{-1} M to 1.0 \times 10^{-6} M of Pb^{2+}$ and its slope (26.5 mV/decade) was near to the sub-Nernstian response in deionized water. Also, the potential was maintained constantly in the range of pH $4.00 \sim 12.00$, which supports the potential usage as $Pb^{2+}$ affinitive electrode in the deionized water.

• Membrane Journal
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• v.3 no.3
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• pp.126-135
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• 1993

Perchlorate ion-selective PVC membrane electrode responsive to $10^{-6}M$ was developed by incorporating the ion-pair complex of perchlorate with the quaternary ammonium salts as a active material. The effect of chemical structure, the content of active material, the kinds of plasticizers, and the membrane thickness on the electrode characteristics such as the linear response range and Nernstian slope of the electrode were studied. With the results, the useful pH range and the selectivity coefficients to various interfering anions were compared and investigated. It was obtained that the effect of the chemical structure of an active material on the electrode characteristics was improved with increasing the alkyl chain length of the quarternary ammonium salts in the ascending order of Aliquat 336P, TOAP, TDAP, and TDDAP. The electrode characteristics was improved with the decrease of the active material content below the optimum membrane composition, and DBP was the best as a plasticizer. The optimum membrane composition was 9.09wt% of TDDAP, 30.3wt% of PVC, and 60.6wt% of ptasticizer(DBP). And the optimum membrane thickness was0.45mm at this composition. Under the above condition, thelinear response ranger was $10^{-1}~1.2 {\times} 10^{-6}M$, and the detection limit was $5.1{\times}10^{-7}M$ with the Nernstian slope of 57mV/decade of activity of perchlorate ion. The electrode potential was stable within the pH range from 4 to 11. The selectivity coefficient was as shown below : $SCN^->I^->NO_3^->Br^->ClO_3^->F^->Cl^->SO_4^{2-}$

• Applied Chemistry for Engineering
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• v.23 no.5
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• pp.474-479
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• 2012

Possibility of the selective removal of $Ca^{2+}$ ions from a mixed solution of $Na^{+}$ and $Ca^{2+}$ ions using membrane capacitive deionization (MCDI) was investigated. Adsorption equilibrium experiments were conducted to determine the selectivity of the CMX cation-exchange membrane toward $Ca^{2+}$ ions. In addition, desalination experiments for a mixed solution (5 meq/L NaCl + 2 meq/L $CaCl_{2}$) were performed using an MCDI cell. The adsorption equilibrium of CMX membrane showed that the equivalent fraction of $Ca^{2+}$ ions in the solution and the CMX membrane were 28.6 and 87.2%, respectively, which indicates the CMX membrane's high selectivity toward $Ca^{2+}$ ions. Desalination experiments were performed by applying a constant current to the MCDI cell until the cell potential reached 1.0 V. The amount of ions adsorbed did not significantly change as the applied current was changed. However, the equivalent fractions of $Ca^{2+}$ ions among the adsorbed ions were inversely proportional to the applied currents: 81.4, 78.4, 77.0, and 74.5% at 200, 300, 500, and $700\;A/m^{2}$ of applied current density, respectively. This result is attributed to the increased fraction of $Ca^{2+}$ ions adsorbed by the CMX membrane at lower applied current densities.