• Proceedings of the KSRS Conference
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• 2008.03a
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• pp.39-43
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• 2008

경관을 구성하는 다양한 요소들의 공간적 분포 패턴과 상호 관계를 정량적으로 분석하기 위하여 다양한 경관지수가 개발되어 사용되고 있다. 경관구조 및 변화특성을 정량적으로 해석하기 위한 노력은 1950년대 후반부터 기하학적 이론을 기초로 하여 제기되어 왔으며, 최근에는 원격탐사, GIS, 정보이론, 프랙탈 이론에 근거한 지표 등이 도입되어 사용되고 있다. 본 연구에서는 연안습지 식생의 발달과 분포 특성을 공간적으로 해석하기 위해 Landsat 영상에 분광혼합분석 기법을 적용하여 선정한 지표면 식생비율을 10개 클래스로 구분한 후 각 클래스에 대해 경관지수를 적용하여 식생비율의 시-공간적 변동 특성을 분석하였다. 새만금방조제를 비롯한 많은 연안습지에 생성되는 습지식생의 공간적 분포를 변화탐지 하고 이들의 시-공간적 분포에 영향을 미치는 요인을 해석하여 연안습지의 보존과 개발에 대한 기초 정보를 위성자료를 통해 추출 분석하였다.

• Analytical Science and Technology
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• v.10 no.3
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• pp.209-215
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• 1997

Li-AGICs as a anode of secondary battery were synthesized by high-pressure method as a function of the Li-contents. The characteristics of these prepared compounds were determined from the studies with X-ray diffraction method, UV/VIS spectrophotometric and differential scanning calorimeter(DSC) analysis. From the results of X-ray diffraction, it was found that the lower stage intercalation compounds were formed with increase of Li-contents. The mixed stages in these compounds were also observed. In the case of the $Li_{30wt%}$-AGIC, the compounds in the stage 1 structure were formed predominantly, but the structure of only pure stage 1 for structural defect of artificial graphite is not observed. According to UV/VIS spectrophotometric analysis, $Li_{30wt%}$-AGIC shows distinguishable energy state spectrum with the position of $R(%)_{min}$ values, but the characteristic spectra of almost all Li-AGICs are not observed. The enthalpy and entropy changes of the compounds can be obtained from the differential scanning calorimetric analysis results. From the results, it was found that exothermic and endothermic reactions of Li-AGICs are related to thermal stability of lithium between artificial graphite layers.

• Korean Chemical Engineering Research
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• v.55 no.3
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• pp.353-357
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• 2017

In this study, the inclusion phenomena of tetrahydrofuran + 3-hydroxytetrahydrofuran + $CH_4$ clathrate hydrates were explored via thermodynamic and spectroscopic approaches. The phase equilibria of the double hydrates - THF + $CH_4$ and 3-OH THF + $CH_4$ clathrate hydrates - were determined by pressure-temperature trace during hydrate formation and dissociation, and the result revealed that the equilibrium pressures were shifted to lower pressure region compared to pure $CH_4$ hydrate. The powder X-ray diffraction patterns revealed that the double hydrates of THF + 3-OH THF formed structure II type clathrate hydrates with $CH_4$. The dispersive Raman spectra of the double clathrate hydrates also exhibited that $CH_4$ can be trapped in both $5^{12}6^4$ and $5^{12}$ cages whereas THF and 3-OH THF were encaged in $5^{12}6^4$ cage.

• Analytical Science and Technology
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• v.15 no.4
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• pp.373-380
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• 2002

Humic and fulvic acids present in soil of different depth were extracted and their characteristics were analyzed as a basic study to evaluate the effect of humic substances on the behaviour of radioactive elements deposited on soil. Molecular size distribution of the humic and fulvic acids was measured by stirred cell ultrafiltration technique and the structural informations were obtained from their UV-Vis., IR and synchronous fluorescence (SyF) spectral analysis. Main molecular size ranges of the soil 1) humic and fulvic acids were 30~100 kDa (46~56%) and 10~30 kDa (33~43%) respectively, and their overall molecular sizes were found to became smaller with increasing the soil depth. Absorptivities measured at 280 nm in the UV-Visible spectra of humic acids were 1.4~1.5 times higher than those of fulvic acids, and increased with increasing the soil depth. SyF spectral data showed two distinct peak components having maximum peak positions of 428 nm (type I) and 498 nm (type II) for the soil humic and fulvic acids. From the analysis of the peak components, it was found that humic molecules are mainly made up of aromatic compounds corresponding to longer wavelength (type II), and the molecular components increased with increasing the soil depth. Analysis of IR spectral data indicated that the humic molecules contain a higher relative concentration of carboxylic groups than those of fulvic molecules, and the carboxylic group contents are seen to increase as the soil depth increase.

• Journal of the Mineralogical Society of Korea
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• v.22 no.2
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• pp.81-86
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• 2009

The luminescence and fluorescence were investigated by photoluminescence spectroscopy for six gemstones which exhibit color change effect. The shape of luminescence peaks appears different when observed by a photoluminescence spectroscopewith a 514 nm Ar laser source. However, it was not possible to observe the difference in the spectra between the natural and synthetic origins for the same type of gemstones. It was found that the photoluminescence spectrum was related to the crystal structure of the stones. Photoluminescence spectra using a 325 nm He-Cd source reveal that fluorescence is relatively strong for synthetic alexandrite, synthetic color change sapphire and natural alexandrite comparing to the rest of gemstones examined.

• Analytical Science and Technology
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• v.15 no.4
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• pp.341-345
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• 2002

The extent of UV-curing photo-polymerization reaction was monitored by near-IR spectroscopic method. Acrylates containing quaternary ammonium salts and Darocur 1173 were used as reactive monomer and a photo initiator, respectively. The extent of photo-polymerization reaction was obtained from the conversion ratio of acrylate double bond calculated from the intensities of measured bands at 1615 nm and at 2105 nm. Near-IR spectroscopic methods can be an useful tool for the monitoring of the progress of photo-polymerization.

• Journal of Korean Society of Environmental Engineers
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• v.35 no.6
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• pp.442-448
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• 2013

There are two approaches in measuring colors (or chromaticity) in water, i.e., visual comparison method and spectrophotometric method. The color of sample was determined by comparing with that of platinum-cobalt standard solution in the visual comparison method. Single or multiple wavelengths are used for the spectrophotometric method. As the accuracy and precision of visual comparison method depend on the eye sight of the analyzer, the results are not so reliable and representative. In addition, it is hard to measure chromaticity less than 5 TCU. Single wavelength approach in spectrophotometric method, can be applied for groundwater or surface water with natural organic matter (i.e., humic substances) while it's hard to measure the color of wastewater which includes anthropogenic chemical compounds. The measurements with multiple wavelengths approach resulted in reliable data regardless of the source of sample water, i.e., surface water and wastewater. As dozens of measurements and complicated calculations for one sample were required for the multiple wavelengths approach, the approach could not be applied for field measurement. In the present study, the authors tested efficient method which could measure the color of water sample accurately and precisely regardless of the source of water. With the colorimeter with multiple wavelengths and calculation program, the colors of water samples could be measured within 3~4 seconds with accuracy and precision.

• Analytical Science and Technology
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• v.12 no.6
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• pp.515-520
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• 1999

The spectrophotometric determination of Al(III) with thorin have been investigated. The optimum condition of pH, concentration of ligand and surfactant, and stability were evaluated. The thorin ligand offers selective separation of Al(III) from sample solution containing Fe(III), Ni(II), Cu(II), Pb(II) and Cu(II). Various surfactants were tested and Triton X-100 showed the best stability and the maximum absorbance in an aqueous solution of Al(III)-Thorin-Triton X-100 complex appears about 526 nm. The method was applied for the determination of Al(III) in mixed sample solution. Separation and preconcentration was performed with a short column filled with resorcinol-formaldehyde resin. Control of the pH during the column operation is essential because the adsorption capacities are very sensitive to change in pH. Their separation was carried out in 0.2 M acetic acid-sodium acetate buffer solution (pH 4.5) and 1.0 M $HNO_3$media.

• Journal of the Korean Chemical Society
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• v.36 no.1
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• pp.107-112
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• 1992

Electron injection from excited rose bengal into the conduction band of a thin film of $SnO_2$ semiconductor in acetonitrile was investigated in an electrochemical cell, ITO/$SnO_2$/rose bengal, NaI or $I_2$, $NaClO_4$/Pt. It was observed that NaI enhanced the supersensitized photocurrent, followed by the slow reduction, whereas $I_2$ yielded a fast decaying photocurrent. Spectroscopic analyses of the dye solution containing NaI revealed that electron is transferred to the $SnO_2$ electrode from the reduced rose bengal and iodide is responsible for the reduction of the dye in triplet state. However $I_2$ appears to possess neither the reducing ability of the oxidized dye nor the retardation of the dehalogenation of RB.

• KSBB Journal
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• v.22 no.2
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• pp.84-90
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• 2007

Trehalose is non-reducing disaccharide which is found in bacteria, fungi, plants and insects. Trehalose has been determined by several analysis methods. To monitor the concentrations of trehalose in a process, enzymatic methods have more advantage over others, e.g. more specific. In this work, trehalase was immobilized on VA-epoxy polymer and applied to FIA systems. The behaviours of these FIA systems were characterized and used to monitor the trehalose concentrations. Use of optical detection technique was chosen for trehalose-FIA system. On-line monitoring data and off-line data were measured by HPLC.