• 한국자기공명학회논문지
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• 제9권2호
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• pp.138-154
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• 2005

Vanadium-incorporated aluminophosphate molecular sieve $VO^{2+}-SAPO-5$ was studied by electron spin resonance (ESR) and electron spin echo modulation (ESEM) spectroscopies to determine the vanadium structure and interaction with various adsorbate molecules. It was found that the main species at low concentration of vanadium is a monomeric vanadium units in square pyramidal or distorted octahedral coordination, both in oxidation state (IV) for the calcined hydrated material and in oxidation state (V) for the calcined material. After calcinations in $O_2$ and exposure to moisture, only species A is observed with reduced intensities. It is suggested as a $VO(H_2O)_3^{2+}$ complex coordinated to two framework oxygen bonded aluminum. When calcined, hydrated $VO^{2+}-}SAPO-5$ is dehydrated at elevated temperature, a species loses its water ligands and transforms to $VO^{2+}$ ions coordinated to two framework oxygens (species B). Species B reduces its intensity, significantly after treatment with $O_2\;at\;600^{\circ}C$ for 5 h, thus suggesting oxidation of $V^{4+}\;to\;V^{5+}$. When dehydrated $VO^{2+}-SAPO-5$ contacts with $D_2O$ at room temperature, the EPR signal of species A is observed. Thus species assumed as a $VO^{2+}(O_f)_2(D_2O)_3$, by considering two framework oxygens. Adsorption of deuterated ethanol, propanol on dehydrated $VO^{2+}_{-}SAPO-5$ result in another new vanadium species E and F, respectively, which are identified as a $VO^{2+}-(CH_3CH_2OD)_3,\;VO^{2+}-(CH_3CH_2CH_2OD)_2$ complex. When deuterated benzene is adsorbed on dehydrated $VO^{2+}-SAPO-5$, another new vanadium species G, identified as a $VO^{2+}-(C_6D_6)$ is observed. Possible coordination geometries of these various complexes are discussed.

• 공업화학
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• 제29권6호
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• pp.657-662
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• 2018

본 연구에서는, $Pt/TiO_2$ 촉매의 물리화학적 특성이 CO 상온산화 반응에 미치는 영향을 조사하기 위하여 각기 다른 물리적 특성을 가지는 다양한 $TiO_2$ 지지체를 이용하여 $Pt/TiO_2$ 촉매를 제조한 후 평가하였다. 촉매의 물리화학적 특성을 조사하기 위하여 XPS, CO-chemisorption, BET, CO-TPD 분석을 수행하였다. 그 결과, active particle diameter가 작을수록, metal dispersion, surface area가 클수록 우수한 CO 상온산화 반응을 나타내었다. 이러한 물리적 특성은 active site의 수를 증진시켜 대상물질은 CO의 흡착량의 증가를 야기시켰다. 또한, $O_2$-consumption이 클수록 우수한 산소 전달 능력을 통해 보다 높은 CO 상온산화 반응활성을 나타내었다.

• 융합정보논문지
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• 제9권2호
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• pp.34-42
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• 2019

본 연구에서는 자동제어시스템이 리액터 운전에 미치는 영향을 분석해 보았다. Propylene 리액터 공정은 복잡하게 구성되어 일반적으로 효율이 낮고, 생산성이 떨어지는 문제로 인해 경제적 손실이 많다. 본 연구에서는 장애요인을 보완하여 운전효율을 높이고, 생산성을 향상시키는 목적으로 연구 모델을 제시하였다. 기존 공정의 구성을 분석하여 하드웨어 시스템 및 소프트웨어 시스템을 독창성 있는 모델로 보완하였다. 설비의 구성을 연간 60 만톤/Year 프로플린을 생산하는 리액터 8기를 기준으로 적용하였다. 연구 모델 적용결과 운전 효율이 높아졌고, 안정성 91%과 더불어 생산량이 90~95% 으로 증가하였다. 향후 연구는 생산성 100% 향상을 위한 연구모델을 제시할 예정이다. 추가적으로 프로플린 부산물인 수소 생산공정인 PSA 시스템의 안정성과 생산성 향상 방안에 대해 연구하고자 한다.

• 공업화학
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• 제22권3호
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• pp.308-311
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• 2011

하수슬러지 촤에 MnOx를 담지한 촉매를 사용하여 $NH_3$를 환원제로 하는 선택적 촉매 환원반응의 반응 메커니즘 분석을 수행하였다. XRD 분석 결과 활성 Mn phase는 $Mn_3O_4$인 것으로 여겨졌다. 또한 $150^{\circ}C$ 이하에서는 흡착반응이 주요한 질소산화물 저감 메커니즘으로 작동하였으나, $100{\sim}150^{\circ}C$에서는 환원반응도 질소산화물 저감에 관여하는 것으로 보여졌다. 실험결과에 기초하여 활성 촤와 여기에 MnOx를 담지한 촤에서의 반응속도상수를 비교하였다. MnOx 담지촤는 높은 충돌계수와 낮은 활성화 에너지에 기인하여 높은 반응속도 상수와 높은 NOx 제거 효율을 나타내었다. 두 가지 촤 모두 본 실험 조건하에서 활성화 에너지는 상대적으로 낮았다(10~12 kJ/mol).

• 한국전기전자재료학회논문지
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• 제34권5호
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• pp.314-320
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• 2021

Controlling ambient humid condition through high performance humidity sensors has become important for various fields, including industrial process, food storage, and the preservation of historic remains. Although aerosol deposited humidity sensors using ceramic BaTiO₃ (BT) material have been widely studied because of their longtime stability, there remain critical disadvantages, such as low sensitivity, low linearity, and slow response/recovery time in case of the sensors fabricated at room temperature. To achieve superior humidity sensing properties even at room temperature condition, BT-Cu composite films utilizing aerosol deposition (AD) process have been proposed based on the percolation theory. The BT-Cu composite films showed gradually improved sensing properties until the Cu concentration reached 15 wt% in the composite film. However, the excessive Cu (above 30 wt%) containing BT-Cu composite films showed a rapid decrease of the sensing properties. The results of observed surface morphology of the AD fabricated composite films, to figure out the metal filler effect, showed correlation between surface topography as well as size and the amount of open pores according to the metal filler content. Overall, it is very important not only dielectric constant of the humidity sensing films but also microstructures, because they affect either the variation range of capacitance by ambient humidity or adsorption/desorption of ambient humidity onto/from the humidity sensing films.

• 멤브레인
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• 제32권2호
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• pp.100-108
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• 2022

다양한 산업 중에서 섬유 산업은 섬유 염색을 위해 가장 많은 양의 물을 사용하는데, 이는 여러 종류의 염료를 포함한 폐수의 방대한 배출로 이어진다. 염료의 제거를 위한 방법에는 오존 처리, 흡착 등의 다양한 처리 방법이 존재한다. 하지만 이러한 처리 방법은 폐수 재사용의 문제로 인해 처리 가격이 상승하기 때문에 성공적이지 못하다. 이에 대한 대안으로 막분리 공정이 폐수의 염료 처리를 위한 가장 적절한 기술로 보고되고 있다. 이때 사용되는 분리막은 고분자 분리막과 세라믹 분리막으로 나눌 수 있다. 세라믹 분리막의 장점에는 세척의 용이함, 긴 수명, 내열성, 내화학성, 그리고 기계적 안정성이 있다. 세라믹 분리막은 다양한 원료로 만들 수 있으며, 점토, 제올라이트, 플라이 애시와 같은 천연 재료는 저렴하고 구하기 용이하다. 본 리뷰에서 폐수처리는 크게 한외여과(ultrafiltration), 정밀여과(microfiltration), 그리고 나노여과(nanofiltration) 세가지 공정으로 나누어져 있다.

• 멤브레인
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• 제32권3호
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• pp.181-190
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• 2022

막여과는 흡착, 응집 등의 폐수 처리 방법에 비교해 경제적이며, 높은 효율을 보인다는 장점을 가지고 있다. 하지만, 막의 표면에 오염물질이 흡착하여 발생하는 막오염 현상으로 인해 막여과의 효율이 크게 줄어들게 된다. 다양한 종류의 막 중에서 세라믹 분리막은 친수성을 띄며, 화학적으로 안정되었기 때문에 오염방지에 효과적이다. 또한, 산화 그래핀 등을 활용한 복합막도 막오염을 예방하는 데 도움이 될 수 있다. 최근에는 막오염을 방지하고 시너지 효과를 얻기 위해 광촉매 분리막이 해결책으로 제시되었다. 막 분리는 광촉매의 단점인 촉매의 낮은 재사용률을 보완할 수 있으며, 광촉매 반응은 오염을 막을 수 있다.

• 청정기술
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• 제28권2호
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• pp.147-154
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• 2022

Titanate nanotubes (TNTs) were synthesized via alkaline hydrothermal treatment using commercial TiO₂ nanoparticles (P25). The TNTs were prepared at various TiO₂/NaOH ratios, hydrothermal temperatures, and hydrothermal times. The synthesized catalysts were characterized by X-ray diffraction, field-emission scanning electron microscopy, N₂ adsorption-desorption isotherms, field-emission transmission electron microscopy, and ultraviolet-visible spectroscopy. TNTs were generated upon a decrease in the TiO₂/NaOH ratio due to the dissolution of TiO₂ in the alkaline solution and the generation of new Ti-O-Ti bonds to form titanate nanoplates and nanotubes. The hydrothermal treatment temperature and time were important factors for promoting the nucleation and growth of TNTs. The TNT catalyst with the largest surface area (389.32 m² g^-1) was obtained with a TiO₂/NaOH ratio of 0.25, a hydrothermal treatment temperature of 130 ℃, and a hydrothermal treatment time of 36 h. Additionally, we investigated the photocatalytic activity of methyl violet 2B (MV) over the TNT catalysts under UV irradiation and found that the degradation efficiencies of the TNTs were higher than that of P25. Among the TNT catalysts, the TNT catalyst that was hydrothermally synthesized for 36 h (TNT 36 h) exhibited a 96.9% degradation efficiency and a degradation rate constant that was 4.8 times higher than P25 due to its large surface area, which allowed for more contact between the MV molecules and TNT surfaces and facilitated rapid electron transfer. Finally, these results were correlated with the specific surface area.

• Nuclear Engineering and Technology
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• 제55권2호
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• pp.516-522
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• 2023

The co-precipitation process plays a key role in the decontamination of radionuclides from low and intermediate levels of liquid waste. For that reason, the removal of Cs ions from waste solution by the co-precipitation method was carried out. A simulated liquid waste (¹³³Cs) was prepared from a 0.1 M CsCl solution, while wastewater generated by washing steel ash served as a representative of radioactive cesium solution (¹³⁷Cs). By co-precipitation, potassium ferrocyanide was applied for the adsorption of Cs ions, while nickel nitrate and iron sulfate were selected for supporting the precipitation. The amount of residual Cs ions in the CsCl solution after precipitation and filtration was determined by ICP-OES, while the radioactivity of ¹³⁷Cs was measured using a gamma-ray spectrometer. After cesium removal, the amount of cesium appearing in both XRD and SEM-EDS was analyzed. The removal efficiency of ¹³³Cs was 60.21% and 51.86% for nickel nitrate and iron sulfate, respectively. For the ash-washing solution, the removal efficiency of ¹³⁷Cs was revealed to be more than 99.91% by both chemical agents. This implied that the co-precipitation process is an excellent strategy for the effective removal of radioactive cesium in waste solution treatment.

• 한국재료학회지
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• 제33권10호
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• pp.430-438
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• 2023

In this study, we synthesized pH-controlled resorcinol-formaldehyde (RF) gels through the polymerization of two starting materials: resorcinol and formaldehyde. The prepared RF gels were dried using an acetone substitution method, and they were subsequently carbonized under nitrogen atmosphere to obtain carbon xerogels (CX_Y) prepared at different pH (Y). The carbon xerogels were utilized as active materials for coin-type organic supercapacitor electrodes to investigate the influence of pH on the electrochemical properties of the carbon xerogels. The carbon xerogels prepared at lower pH (CX_9.5 and CX_10) exhibited sufficient particle growth, with a three-dimensional network of particles during the RF gel formation, resulting in the development of abundant mesopores. Conversely, the carbon xerogels prepared at higher pH (CX_11 and CX_12) retained densely packed structures of small particles, leading to pore collapse and low specific surface areas. Consequently, CX_9.5 and CX_10 showed high specific surface areas, and provided ample adsorption sites for the formation of electric double layers with electrolyte ions. Moreover, the three-dimensional particle network in CX_9.5 and CX_10 significantly enhanced electrical conductivity. The presence of well-developed mesopores in these materials further facilitated the effective transport of electrolyte ions, contributing to their superior performance as organic supercapacitor electrodes. This study confirmed that pH-controlled carbon xerogels are one of the promising active materials for organic supercapacitor electrodes. Furthermore, we concluded that pH during RF gel formation is a crucial factor determining the electrode performance of the carbon xerogels, highlighting the need for precise pH control to obtain high-performance carbon xerogel electrodes.