• Journal of the Korean Chemical Society
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• v.43 no.2
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• pp.167-171
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• 1999

An investigation of the interaction of Co(II), Ni(II), Cu(II), Zn(II), Cd(II), Pb(II) and Ag(I) with two N,N'-dibenzylated nitrogen-oxygen mixed donor macrocyclic ligands, has been carried out. Tle log K values for the respective complexes in 95% methanol have been determined potentiometrically. Both ligands have formed stable complex with only Cu(II) and Ag(I) ion. Transport measurements in a bulk liquid membrane system exhibited a very high selectivity of Ag(I) ion over the other metal ions used.

• Analytical Science and Technology
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• v.5 no.1
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• pp.33-39
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• 1992

THF-based crown-4 of 16-membered rings having tetrahydrofuran unit was synthesized by an acid-catalyzed condensation of furan and acetone followed by hydrogenation in an effort to obtain highly elective ionophores for lithium ions. The new ionophore was compared with previously reported ionophores under similar measurement conditions with the same plasticizer, tris(2-ethylhexyl) phosphate in poly(vinyl chloride)(PVC) membrane electrodes. Separate solution method was used to determine relative selectivity coefficients for the electrode. The selectivity coefficients($K_{LiM}^{POT}$) of lithium over ammonium, alkali and alkaline earth metal ions go from about $2.4{\times}10^{-1}$ to $2.3{\times}10^{-4}$ to working range and pH dependence have also been studied.

• Journal of the Korea Institute of Military Science and Technology
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• v.16 no.5
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• pp.690-702
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• 2013

Ionic liquids(ILs) have been the most investigated chemicals among green solvents including water, glycerol, supercritical carbon dioxdie($scCO_2$). ILs are attracting organic as well as inorganic chemicals because most ionic liquids' vapor pressures are very low so that ILs are liquids phase at ambient conditions. ILs are composed of various anions and cations, thus chemists can design functionalized solvents and/or catalysts that can be used in specific synthetic reactions by means of combinations of different ions. Many scientists believe ILs being green materials because of its low vapor pressure as well as the flexibility in controlling the chemical and physical properties. In this review the author describes recent development of ILs focused on imidazolium and pyridinium ILs which are being most investigated presently. In order to apply this materials in industrial level, the toxicity matter must be resolved first. In this regard, the author describes recent research trend regarding environmental effects by ILs as well as some meaningful results as well.

• Applied Chemistry for Engineering
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• v.24 no.5
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• pp.443-455
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• 2013

Electrochemical studies on charge transfer reactions across the interface between two immiscible electrolyte solutions (ITIES) have greatly attracted researcher's attentions due to their wide applicability in research fields such as ion sensing and biosensing, modeling of biomembranes, pharmacokinetics, phase-transfer catalysis, fuel generation and solar energy conversion. In particular, there have been extensive efforts made on developing sensing platforms for ionic species and biomolecules via gelifying one of the liquid phases to improve mechanical stability in addition to creating microscale interfaces to reduce ohmic loss. In this review, we will mainly discuss on the basic principles, applications and future aspects of various sensing platforms utilizing ion transfer reactions across the ITIES. The ITIES is classified into four types : (i) a conventional liquid/liquid interface, (ii) a micropipette supported liquid/liquid interface, (iii) a single microhole or an array of microholes supported liquid/ liquid interface on a thin polymer film, and (iv) a microhole array liquid/liquid interface on a silicon membrane. Research efforts on developing ion selective sensors for water pollutants as well as biomolecule sensors will be highlighted based on the use of direct and assisted ion transfer reactions across these different ITIES configurations.

• Journal of the Korean Vacuum Society
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• v.3 no.2
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• pp.158-165
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• 1994

액체금속 이온 소오스의 모양에 대한 개선된 원추 모델을 제시하였다. 이 모델에서는 전도성 유 체의 테일러 원추를 0차 모양으로 하고 원추에서 벗어난 변형을 전자유체 역학적으로 취급하였다. 외부 의 전기적 스트레스 때문에 원추정점에서 일어나는 돌출을 오직 ra인 영역에서는 변형 이 없다는 것으로 정의되는 값이다. 이 가정에 의하여 각변형ζ는 다음같은 형태를 가졌다: r$\varepsilon$(t)이고 r>adlsrudn는 ζ=(a/r)$\varepsilon$이다. 여기서 지수 s는 변형의 모양을 나타내는 값이다. 이것을 모양방정식에 대입하여 계산한 결과 모양의 불안정되는 전위값은 Vc(r, h)=V0(h) V1은 1차의 표 면이 불안정되는 전위값으로 이온방출을 일어나는데 필요한 여분 값이다. 이렇게 얻어진 이온방출의 임 계전위 Vc는 실험치와 부합되는 값이었다. 더욱 중요한 것은 위의 Vc 형태가 국지불안정을 설명하여 주었다. 또한 외부에서 걸어준 전위가 임계전위값을 넘을 때 각변형 ζ>0이고 )

• Applied Chemistry for Engineering
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• v.24 no.4
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• pp.412-415
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• 2013

Palladium on carbon powder was prepared using 1-hexyl-3-methylimidazolium tetrafluoroborate, one of room temperature ionic liquids. The synthesized particles were tested as a hexafluoropropylene hydrogenation catalyst. Moreover, the hydrogenation was performed under various reaction conditions to develop an optimum reaction process. The catalyst prepared by more than 3 wt% of palladium and the unity mole ratio of ionic liquid to palladium precursor showed higher catalytic activity. For reaction conditions, the complete hexafluoropropylene (HFP) conversion was achieved at these conditions; the volume flow ratio of hydrogen to HFP was higher than 1.25 and $GHSV_{HFP}$ was lower than 50000 mL/g-h.

• Proceedings of the Korean Radioactive Waste Society Conference
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• 2015.10a
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• pp.327-328
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• 2015

• Proceedings of the Korean Radioactive Waste Society Conference
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• 2016.10a
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• pp.375-376
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• 2016

• Proceedings of the Korean Radioactive Waste Society Conference
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• 2015.10a
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• pp.363-364
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• 2015

• Proceedings of the Korean Radioactive Waste Society Conference
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• 2016.05a
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• pp.251-252
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• 2016