• Korean Journal of Optics and Photonics
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• v.11 no.5
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• pp.335-339
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• 2000

A $1.31/1.55\mu\textrm{m}$ coarse WDM opncal dIrectional coupler that conslsls of two idenlical straight channel waveguides in BK7 glass has been fabricated. The separatIOn between two channel waveguides is $8\mu\textrm{m}$ and the wavegu.ide width is $4\mu\textrm{m}$ . Especlally, we assumed that the index profile is Gaussian function and complementary error function in the width direction and depth direction, respectrvely. This directional coupler operating at $1.31/1.55\mu\textrm{m}$ with crosstalk of 18dB is demonstrated and has the 16 mm long length with 12.6 mm coupling region.region.

• Proceedings of the Optical Society of Korea Conference
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• 2000.08a
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• pp.158-159
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• 2000

본 논문에서는 BK7 유리 기판에 Ag$^{+}$-$Na^{+}$ 이온교환법을 이용하여 1.31/1.55$mu extrm{m}$ 방향성 광결합기형 역다중화기를 제작하여 특성을 평가하였다. BK7에 이온교환법을 이용하여 도파로를 제작할 경우 0.2dB/cm 이하의 전파손실을 유지할 수 있으며 또한 도파로의 굴절율 분포가 단일모드 광섬유와 매우 유사하여 광섬유와 광소자 사이의 접합면에서 발생하는 접합손실을 줄일 수 있다 또한 BK7을 이용하면 도파로를 제작하였을 때 복굴절 현상이나 편광 의존성이 적어서 수동 소자 제작에 유용하다는 장점이 있다$^{(1 3)}$ . (중략)

• Proceedings of the Membrane Society of Korea Conference
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• 1994.10a
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• pp.84-85
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• 1994

본 연구는 수용상에 포함된 중금속이온중 에멀젼 액막법(Emulsion Liquid Membranes, ELM)을 이용하여 납이온을 제거시키기 위한 연구이다. 지금까지 수용액상의 중금속 이온의 제거는 전통적으로 이온 침전법을 사용하여 왔다. 그러나 이 방법은 스럿지 처리문제가 남아 있고 식수로 이용되는 수처리에는 식수기준 만족도 때문데 적합하지 않았다. ELM법에 의한 금속이온 제거처리는 전기도금에 의하여 중금속이온을 회수할 수 있고 고도의 수처리를 가능케하여 최근 많은 관심을 갖고 있다. 본 연구에서는 납 이온 추출제로서 D2EPHA와 Alamine336의 이온교환제를 사용하여, 이 씨스테므이 추출 평형자료를 구하고 pH, 추출제의 농도, 교반속도, 에멀젼비율등에 의한 추출효과등을 검토하였다. 또한 2단계 추출 방법을 사용하여 금속이온추출에서 가장 큰 문제점인 유기상 용액의 leakage를 해결하고자 하였다.

• 대한방사선방어학회:학술대회논문집
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• 2011.11a
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• pp.332-333
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• 2011

• Korean Journal of Optics and Photonics
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• v.3 no.3
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• pp.198-202
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• 1992

Silver ion-exchanged glass waveguide with its large surface index difference and shallow depth is suitable to be used for the hybrid integration of semiconductor device and glass waveguide using the semiconductor film grafting technique. We report characteristics of the planar and channel glass waveguides exchanged in the diluted silver nitrate melt in the visible and infrared spectral region. Especially, we determined the fabrication parameters for single-mode channel waveguide at 1.5.$\mu$m, an important wavelength in the optical communication. Directional couplers with several different configurations were fabricated, and their 3 dB coupling length was determined as a function of wavelenGh and polarization.

• Applied Chemistry for Engineering
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• v.10 no.6
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• pp.871-875
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• 1999

We calculated the characteristics of a phosphoric cation exchanger and studied on an accurately computable method to determine the ion exchange capacity for type of potentiometric titration curve. The ion exchanger was prepared by phosphorylation of a styrene-divinylbenzene copolymer with 4% crosslinking. The ion exchange capacity is 5.7 meq/g. The experimental pK values versus ${\mathit{x}}$ in phosphoric cation exchanger can be expressed as a linear equation. The ${\Delta}pK$ values were obtained from the slope of linear equation. The ${\Delta}pK$ values are the differences of antilogarithms(pK) values of the apparent equilibrium constant at complete and zeroth neutralization of the ion exchanger. Also the experimental pK values at ${\mathit{x}}=0.5$ were accorded well with theoretical data. And when it is titrated with NaOH and $Ba(OH)_2$ solutions, a good agreement between experimental and theoretical pK values for various ${\mathit{x}}$ was seen in all the potentiometric titration curves. We knew that the inflection point of potentiometric titration curve in the case of divalent ions are changed much large than that for monovalent ions. If the relation between g values and ${\partial}pH/{\partial}g$ was plotted to the Lorentz distribution curve, ion exchange capacity can be accurately evaluated.

• Applied Chemistry for Engineering
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• v.26 no.5
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• pp.575-580
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• 2015

Pd/C catalysts were prepared by various preparation methods such as ion exchange, impregnation and polyol method and also characterized by nitrogen adsorption-desorption isothermal, XRD, FE-TEM and CO-chemisorption. The activities of these catalysts were tested in the hydrogenation of cyclohexene to cyclohexane. Catalytic activities of Pd/C catalysts were found to be effected by the chosen preparation methods. Pd dispersions of each Pd/C catalysts prepared by ion exchange, impregnation and polyol method were 17.55, 13.82% and 1.35%, respectively, confirmed by CO-chemisorption analysis. These were also in good agreement with the FE-TEM results. The Pd/C catalyst prepared by ion exchange method exhibits good performance with the cyclohexene conversion rate of 71% for 15 min. These results indicate that Pd/C catalyst having higher dispersion and lower particle size is in favor of hydrogenation cyclohexene and also Pd dispersion increases with the increment of catalytic activity.

• Journal of the Mineralogical Society of Korea
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• v.15 no.4
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• pp.329-344
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• 2002

Mineralogical and chemical characterization of some domestic bentonites, such as quantitative XRD analysis, chemical leaching experiments, pH and CEC determinations, were done without any separation procedures to understand their relationships among mineral composition, characteristics, and cation exchange properties. XRD quantification results based on Rietveld method reveal that the bentonites contain totally more than 25 wt% of impurities, such as zeolites, opal-CT, and feldspars, in addition to montmorillonite ranging 30～75 wt%. Cation exchange properties of the zeolitic bentonites are deeply affected by the content of zeolites identified as clinoptilolite-heulandite series. Clinoptilolite is common in the silicic bentonites with lighter color. and occurs closely in association with opal-CT. Ca is mostly the dominant exchangeable cation, but some zeolitic bentonites have K as a major exchangeable cation, The values of cation exchange capacity (CEC) determined by Methylene Blue method are comparatively low and have roughly a linear relationship with the montmorillonite content of the bentonite, though the correlated data tend to be rather dispersed. Compared to this, the CEC determined by Ammonium Acetate method, i.e.‘Total CEC’, has much higher values (50～115 meq/100 g). The differences between those CEC values are much greater in zeolitic bentonites, which obviously indicates the CEC increase affected by zeolite. Other impurities such as opal-CT and feldspars seem to affect insignificantly on the CEC of bentonites. When dispersed in distilled water, the pH of bentonites roughly tends to increase up to 9.3 with increasing the alkali abundance, especially Na, in exchangeable cation composition. However, some bentonites exhibit lower pH (5～6) so as to regard as ‘acid clay’. This may be due to the presence of $H^{＋}$ in part as an exchangeable cation in the layer site of montmorillonite. All the works of this study ultimately suggest that an assesment of domestic bentonites in grade and quality should be accomplished through the quantitative XRD analysis and the ‘Total CEC’measurement.

• Proceedings of the Korean Environmental Sciences Society Conference
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• 2003.11b
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• pp.315-318
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• 2003

본 연구에서는 NaCl 용응법에 의해 fly ash로부터 합성된 swelling mica의 다양한 이온의 교환특성과 이온교환이 결정구조에 미치는 영향을 규명함으로서 swelling mica에 의한 유해 방사능 물질 및 중금속의 효과적인 제거제로서의 활용 가능성을 조사하고자 하였다. 1가 양이온이 흡착된 FA-swelling mica의 $d_{001}$/ peak의 강도는 흡착된 이온의 직경이 클수록 감소하는 경향을 나타내었으나, $d_{001}$/ value는 흡착된 이온의 직경과 뚜렷한 상관관계가 없었다. 또한 FA-swelling mica의 NH4 이온의 흡착량은 133 $cmol^{+}$/kg, K 이온은 127 $cmol^{+}$/kg, Li 이온은 23 $cmol^{+}$/kg으로서 방사성 물질과 중금속 이온에 비해 낮은 경향을 나타내었다. 2가 양이온이 흡착된 FA-swelling mica의 $d_{001}$/ peak 강도와 $d_{001}$/ value는 이온의 직경에 관계없이 비슷한 값을 나타내었으며 1가 양이온의 흡착에 비해 구조적 안정성이 높았다. Sr 및 Ba 이온의 흡착반응은 느리고 지속적으로 일어났으며 Ca와 Mg 같은 2가 양이온에 비해 선택성이 훨씬 높은 것으로 나타났다. 또한 Sr 및 Ba 이온과 같이 직경이 큰 방사성 원소들은 swelling mica의 층간에 흡착되어 결정구조가 부분적으로 붕괴됨으로서 이온을 비가역적으로 고정하는 특성을 나타내었다. Zn, Cu, Cd 및 Pb 등의 중금속 이온이 흡착된 FA-swelling mica의 $d_{001}$/ value는 12.70~12.80$\AA$으로서 매우 일정하였으며, 이온 흡착에 의한 층간 팽창정도는 이온의 크기뿐만 아니라 수화정도에 따라 상이하였다. FA-swelling mica의 중금속 이온의 흡착은 층간 붕괴에 의해 일어나는 것으로 판단되며, 선택성과 흡착능력은 층간 붕괴속도와 비례하는 경향을 나타내었다. 또한 FA-swelling mica의 중금속 이온의 선택성은 Pb>Cu>Cd$\geq$Zn 순으로 나타났다.

• Korean Journal of Mineralogy and Petrology
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• v.35 no.1
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• pp.41-50
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• 2022

To study the properties of Sr²⁺ exchange into zeolite A with increasing the molar concentration of Na⁺ in given exchange solution, four single crystals of fully dehydrated Sr²⁺- and Na⁺- exchanged zeolite A were prepared by the bath method using mixed ion-exchange solutions. The Sr(NO₃)₂:NaNO₃ molar rations of the ion exchange solution were 1:1(crystal 1), 1:100(crystal 2), 1:250(crystal 3), and 1:500 (crystal 4), respectively, with a total concentration of 0.05 M. The single-crystals were then vacuum dehydration at 623 K and 1×10^-4 Pa for 2 days. Their single-crystal structures were determined by single-crystal synchrotron X-ray diffraction techniques in the cubic space group Pm3-m, at 100(1) K, and were then refined to the final error indices of R₁/wR₂=0.047/0.146, 0.048/0.142, 0.036/0.128, and 0.040/0.156 for crystals 1, 2, 3, and 4, respectively. In crystals 1 and 2, the 6 Sr²⁺ ions are found at three different crystallographic sites. In crystal 3, 1 Sr²⁺ and 10 Na⁺ ions are found in large cavity and sodalite unit. In crystal 4, only 12 Na⁺ ions occupy three equipoints. The degree of Sr²⁺ ion-exchange decreased sharply from 100 to 16.7 to 0% as the initial Na⁺ concentration increase and the Sr²⁺ concentration decrease. In addition, the unit cell constant of the zeolite framework decreased with this lower level of Sr²⁺ exchange.