Nitrogen-doped carbon nanosheets with a developed porous structure were prepared from polyurethane foams by hydrothermal carbonization following ZnCl2 chemical activation. Scanning electron microscopy, thermogravimetric analysis, Fourier transform infrared spectroscopy, solid state 13C nuclear magnetic resonance (NMR) spectra and X-ray photoelectron spectroscopy were used to characterize the nitrogen-doped carbon nanosheet structure and composition. The removal of Cr(VI) by the N-doped carbon nanosheets was investigated. The results showed that the maximum removal capacity for chromium of 188 mg/g was found at pH=2.0 with PHC-Z-3. pH had an important effect on Cr(VI) removal and the optimal pH was 2.0. Moreover, amino groups and carboxyl groups in the nitrogen-doped carbon nanosheet played important roles in Cr(VI) removal, and promoted the reduction of Cr(VI) to Cr(III).

In this study, a flat-type photocatalytic reactor is applied under solar irradiation for simultaneous treatment of target pollutants: reduction of Cr(VI) to Cr(III) and oxidation of EDCs (BPA, EE2, E2). An immobilized type of photocatalyst was fabricated to have self-grown nanotubes on its surface in order to overcome limitations of powdery photocatalyst. Moreover, Ti mesh form was chosen as substrate and modified to have both larger surface area and photocatalyst content. Ti mesh was anodized at 50V and 25°C for 30min in the mixed electrolytes (NH4F-H2O-C2H6O2) and annealed at 450°C for 2 hours in ambient oxygen to have anatase structure. Surface characterization was done with SEM and XRD methodologies. Fabricated NTT was applied to water treatment, and coexisting Cr(VI) and organics (EDCs) enhanced each other's reactions by scavenging holes and electrons and thus impeding recombination. Also, several experiments were conducted outdoor under direct sunlight and it was observed that both solar-tracking and applying modified photocatalyst were proven to enhance reaction efficiency.

The concern over the risk of environmental exposure to brominated phenols has been increased and has led the researchers to focus their attention on the study of bromophenol treatment. In this study, the effects of pH and ferrate(VI) dose on the degradation of 2-bromophenol were investigated. The results indicated that the oxidation of 2-bromophenol by liquid ferrate(VI) was found to be highly sensitive to the pH condition. Furthermore, the highest removal efficiency was observed at the neutral condition with the removal efficiency of 94.2%. In addition, experimental results showed that 2-bromophenol removal efficiency increased with increasing of ferrate dosage. Ferrate(VI) dose of 0.23 mM was sufficient to remove most of the 2-bromophenol with the efficiency of 99.73% and kapp value of 2982 M-1s-1. Seven compounds were identified as the intermediate products by the GC/MS analysis.

The symbiotic star V1016 Cygni, a detached binary system consisting of a hot white dwarf and a mass-losing Mira variable, shows very broad emission features at around 6825 °A and 7082 °A, which are Raman scattered Ovi  1032, 1038 by atomic hydrogen. In the high resolution spectrum of V1016 Cyg obtained with the Bohyunsan Optical Echelle Spectrograph these broad features exhibit double peak profiles with the red peak stronger than the blue counterpart. However, their profiles differ in such a way that the blue peak of the 7082 feature is relatively weaker than the 6825 counterpart when the two Raman features are normalized to exhibit an equal red peak strength in the Doppler factor space. Assuming that an accretion flow around the white dwarf is responsible for the double peak profiles, we attribute this disparity in the profiles to the local variation of the flux ratio of Ovi  1032, 1038 in the accretion flow. A Monte Carlo technique is adopted to provide emissivity maps showing the local emissivity of Ovi 1032 and Ovi 1038 in the vicinity of the white dwarf. We also present a map indicating the differing flux ratios of Ovi  1032 and 1038. Our result shows that the flux ratio reaches its maximum of 2 in the emission region responsible for the central trough of the Raman feature and that the flux ratio in the inner red emission region is almost 1. The blue emission region and the outer red emission region exhibit an intermediate ratio around 1.5. We conclude that the disparity in the profiles of the two Raman Ovi features strongly implies accretion flow around the white dwarf, which is azimuthally asymmetric.

The degradation characteristics of perchloroethylene by ferrate(VI) oxidation have been studied. The degradation efficiency of perchloroethylene in aqueous solution was investigated at various values of ferrate(VI) dosage, pH, initial concentration of perchloroethylene and aqueous solution temperature. GC-ECD has been used to analyze the changes of perchloroethylene concentration. The optimum conditions of perchloroethylene degradation were obtained at pH 7.0 and 25°C of aqueous solution temperature. Also, the experimental results showed that perchloroethylene removal efficiency increased with the decrease of initial concentration of perchloroethylene. Lastly intermediate products were identified by GC-MS techniques. Trichloroethylene and chloroform were identified as reaction intermediates.

In this study, flat-type photocatalytic reaction system is applied to reduce toxic hexavalent chromium (Cr(VI)) to trivalent chromium (Cr(III)) in aqueous solution under UV irradiation. To overcome the limitation of conventional photocatalysis, a novel approach toward photocatalytic system for reduction of hexavalent chromium including nanotubular TiO2 (NTT) on two kinds of titanium substrates (foil and mesh) were established. In addition, modified Ti substrates were prepared by bending treatment to increase reaction efficiency of Cr(VI) in the flat-type photocatalytic reactor. For the fabrication of NTT on Ti substrates, Ti foil and mesh was anodized with mixed electrolytes (NH4F-H2O-C2H6O2) and then annealed in ambient oxygen. The prepared NTT arrays were uniformly grown on two Ti substrates and surface property measurements were performed through SEM and XRD. Hydraulic retention time(HRT) and substrate type were significantly affected the Cr(VI) reduction. Hence, the photocatalytic Cr(VI) reduction was observed to be highest up to 95% at bended(modified) Ti mesh and lowest HRT. Especially, Ti mesh was more effective as NTT substrate in this research.

목적: 본 연구는 콘택트렌즈 재료로 널리 사용되는 2-hydroxyethyl methacrylate, N-vinyl-2-pyrrolidone, methyl methacrylate, ethylene glycol dimethacrylate에 titanium isopropoxide와 tungsten(VI) oxide 나노입자를 첨가하여 안의료용 렌즈 재료를 중합하였다. 방법: 안의료용 콘택트렌즈의 첨가제로 Tungsten (VI) oxide 나노입자 사용의 활용도를 조사하기 위해 tungsten(VI) oxide 나노입자를 포함한 하이드로젤 콘택트렌즈 재료의 광학적, 물리적 특성 변화를 측정하였다. 결과: 생성된 고분자에 대한 자외선 영역의 투과율은 매우 낮게 측정되어 자외선 차단 능력이 있는 것으로 나타났다. 또한 tungsten(VI) oxide 나노입자의 첨가는 함수율의 큰 변화를 나타내지 않았으나 일정비율을 첨가한 조합에서는 소량의 함수율 변화가 나타났다. 함수율의 큰 변화가 없음에도 불구하고 산소침투율의 측정 값은 tungsten(VI) oxide 나노입자의 첨가 비율이 증가할수록 계속적으로 감소하는 경향이 나타 났다. 결론: 이상의 결과를 통해 titanium isopropoxide 및 tungsten(VI) oxide 나노입자는 하이드로젤 콘택트렌즈의 기본적인 물성을 만족시키면서 기능성 콘택트렌즈 재료로 유용하게 활용될 수 있을 것으로 판단된다.

UV-Vis 분광광도법과 시간분해 레이저 유도 형광분광법(TRLFS)을 이용하여 흄산의 모사 리간드로 사 용한 2,6-Dihydroxybenzoate(DHB)와 U(VI)의 착물형성반응을 조사하였다. U(VI)-DHB 착물 고유의 전 하이동 흡수 스펙트럼을 분석한 결과, 착물형성반응은 우라늄-리간드 비가 1:1 또는 1:2 착물을 형성하는 이중 평형반응이며, 산도에 따라 착물종의 분포가 변한다는 것을 밝혔다. 계산된 착물형성상수 (log K1and log K2)는 12.4±0.1과 11.4±0.1이다. 이에 더하여, TRLFS 방법으로 조사한 결과, DHB는 U(VI) 화 학종들의 형광 소광제(quencher)로서 역할을 한다는 것을 확인하였다. 특히, 확인된 U(VI) 화학종 모두 (UO2 2+, (UO2)2(OH)2 2+과 (UO2)3(OH)5 +)에서 정적 (static) 및 동적 (dynamic) 소광작용이 공존하는 것으 로 관찰되었다. 시간분해 형광 스펙트럼으로부터 리간드 농도에 따른 U(VI) 화학종의 형광세기와 형광수 명을 측정하였으며, Stern-Volmer 식을 이용하여 분석하였다. 결정된 정적소광계수(KS)는 UO2 2+, (UO2)2(OH)2 2+ 과 (UO2)3(OH)5+에 대하여 각각 4.2±0.1, 4.3±0.1 과 4.34±0.08이다. Stern-Volmer 식 을 이용한 분석 결과, 단일 또는 이중 배위자 구조(mono- and bi-dentate)의 U(VI)-DHB 착물이 모두 정 적소광효과에 관여하는 바닥상태 착물임을 확인하였다.