본 연구에서는 배가스 내 존재하는 오염물질인 NO의 처리효율을 증대시키기 위하여 NO 산화 공정을 연구하였으며, 강력한 산화력의 건식산화제를 제조하는 방법으로 H2O2 촉매분해가 도입되었다. H2O2 분해공정 상에서 적용 가능한 K-Mn/Fe2O3 불균일계 촉매가 제조되었으며, 이들이 가지는 물리화학 적 특성이 H2O2 분해반응에 미치는 영향이 조사되었다. 제조된 건식산화제는 NO가 포함된 모사 배가스를 처리하기 위한 NO 산화공정에 적용되었으며, 다양한 모사 배가스의 유량(5, 10, 20 L/min)에서 약 100% 가까운 NO 전환율을 확인 하였다.

This study investigates the oxidation properties of Fe-14Cr ferritic oxide-dispersion-strengthened (ODS) steel at various high temperatures (900, 1000, and 1100°C for 24 h). The initial microstructure shows that no clear structural change occurs even under high-temperature heat treatment, and the average measured grain size is 0.4 and 1.1 μm for the as-fabricated and heat-treated specimens, respectively. Y–Ti–O nanoclusters 10–50 nm in size are observed. High-temperature oxidation results show that the weight increases by 0.27 and 0.29 mg/cm2 for the asfabricated and heat-treated (900°C) specimens, and by 0.47 and 0.50 mg/cm2 for the as-fabricated and heat-treated (1000°C) specimens, respectively. Further, after 24 h oxidation tests, the weight increases by 56.50 and 100.60 mg/cm2 for the as-fabricated and heat-treated (1100°C) specimens, respectively; the latter increase is approximately 100 times higher than that at 1000°C. Observation of the surface after the oxidation test shows that Cr2O3 is the main oxide on a specimen tested at 1000°C, whereas Fe2O3 and Fe3O4 phases also form on a specimen tested at 1100°C, where the weight increases rapidly. The high-temperature oxidation behavior of Fe-14Cr ODS steel is confirmed to be dominated by changes in the Cr2O3 layer and generation of Fe-based oxides through evaporation.

Various morphologies of copper oxide (CuO) have been considered to be of both fundamental and practical importance in the field of electronic materials. In this study, using Cu (0.1 μm and 7 μm) particles, flake-type CuO particles were grown via a wet oxidation method for 5min and 60min at 75 oC. Using the prepared CuO, AlN, and silicone base as reagents, thermal interface material (TIM) compounds were synthesized using a high speed paste mixer. The properties of the thermal compounds prepared using the CuO particles were observed by thermal conductivity and breakdown voltage measurement. Most importantly, the volume of thermal compounds created using CuO particles grown from 0.1 μm Cu particles increased by 192.5% and 125 % depending on the growth time. The composition of CuO was confirmed by X-ray diffraction (XRD) analysis; cross sections of the grown CuO particles were observed using focused ion beam (FIB), field emission scanning electron microscopy (FE-SEM), and energy dispersive analysis by X-ray (EDAX). In addition, the thermal compound dispersion of the Cu and Al elements were observed by X-ray elemental mapping.

In this study, we report the microstructure and the high-temperature oxidation behavior of Fe-Ni alloys by spark plasma sintering. Structural characterization is performed by scanning electron microscopy and X-ray diffraction. The oxidation behavior of Fe-Ni alloys is studied by means of a high-temperature oxidation test at 1000oC in air. The effect of Ni content of Fe-Ni alloys on the microstructure and on the oxidation characteristics is investigated in detail. In the case of Fe-2Ni and Fe-5Ni alloys, the microstructure is a ferrite (α) phase with body centered cubic (BCC) structure, and the microstructure of Fe-10Ni and Fe-20Ni alloys is considered to be a massive martensite (α’) phase with the same BCC structure as that of the ferrite phase. As the Ni content increases, the micro-Vickers hardness of the alloys also increases. It can also be seen that the oxidation resistance is improved by decreasing the thickness of the oxide film.

This study is carried out to obtain basic data regarding oxidation and reduction reactions, originated on the recycling of waste tungsten hard scraps by oxidation and reduction processes. First, it is estimated that the theoretical Gibbs free energy for the formation reaction of WO2 and WO3 are calculated as ΔG1,000K= -407.335 kJ/mol and ΔG1,000K = -585.679 kJ/mol, from the thermodynamics data reported by Ihsan Barin. In the experiments, the oxidation of pure tungsten rod by oxygen is carried out over a temperature range of 700-1,000oC for 1 h, and it is possible to conclude that the oxidation reaction can be represented by a relatively linear relationship. Second, the reduction of WO2 and WO3 powder by hydrogen is also calculated from the same thermodynamics data, and it can be found that it was difficult for the reduction reaction to occur at 1,027oC, in the case of WO2, but it can happen for temperatures higher than 1127oC. On the other hand, WO3 reduction reaction occurs at the relatively low temperature of 827oC. Based on these results, the reduction experiments are carried out at a temperature range of 500-1,000oC for 15 min to 4 h, in the case of WO3 powder, and it is possible to conclude that the reduction at 900oC for 2h is needed for a perfect reduction reaction.

Membrane based water and wastewater treatment becomes more and more popular; however, membrane fouling is still a critical obstacle for its extensive use. Most of the membranes being used are polymeric and have limitations in physical, chemical, and thermal stability, even though various novel materials were introduced. In this study, metal membranes were fabricated to solve those weak points of polymeric membranes. We evaluated the physical properties of a metal membrane, such as pore size distribution, surface morphology, and water flux, and finally used the membrane for electrochemical oxidation of municipal wastewater with simultaneous hydrogen fuel generation. The metal membrane removed 50-70% of the feed organic matter by electrochemical oxidation; 10-30 % removal by electrochemical oxidation plus 40% by membrane rejection.

In this work, we studied the effects of electrochemical oxidation treatments of carbon fibers (CFs) on interfacial adhesion between CF and epoxy resin with various current densities. The surface morphologies and properties of the CFs before and after electrochemical-oxidation-treatment were characterized using field emission scanning electron microscopy, atomic force microscopy, Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, and single-fiber contact angle. The mechanical interfacial shear strength of the CFs/epoxy matrix composites was investigated by using a micro-bond method. From the results, electrochemical oxidation treatment introduced oxygen functional groups and increased roughness on the fiber surface. The mechanical interfacial adhesion strength also showed higher values than that of an untreated CF-reinforced composite.

Polyacrylonitrile (PAN)-based carbon fibers have high specific strength, elastic modulus, thermal resistance, and thermal conductivity. Due to these properties, they have been increasingly widely used in various spheres including leisure, aviation, aerospace, military, and energy applications. However, if exposed to air at high temperatures, they are oxidized, thus weakening the properties of carbon fibers and carbon composite materials. As such, it is important to understand the oxidation reactions of carbon fibers, which are often used as a reinforcement for composite materials. PAN-based carbon fibers T300 and T700 were isothermally oxidized in air, and microstructural changes caused by oxidation reactions were examined. The results showed a decrease in the rate of oxidation with increasing burn-off for both T300 and T700 fibers. The rate of oxidation of T300 fibers was two times faster than that of T700 fibers. The diameter of T700 fibers decreased linearly with increasing burn-off. The diameter of T300 also decreased with increasing burn-off but at slower rates over time. Cross-sectional observations after oxidation reactions revealed hollow cores in the longitudinal direction for both T300 and T700 fibers. The formation of hollow cores after oxidation can be traced to differences in the fabrication process such as the starting material and final heat treatment temperature.

In order to improve the high-temperature oxidation stability, sintered 434L stainless steel is studied, focusing on the effect of the addition of metallic oxides to form stable oxide films on the inner particle surface. The green compacts of Fecralloy powder or amorphous silica are added on STS434L and oxidized at 950oC up to 210 h. The weight change ratio of 434L with amorphous silica is higher than that of 434L mixed with Fecralloy, and the weight increase follows a parabolic law, which implies that the oxide film grows according to oxide diffusion through the densely formed oxide film. In the case of 434L mixed with Fecralloy, the elements in the matrix diffuse through the grain boundaries and form Al2O3 and Fe-Cr oxides. Stable high temperature corrosion resistance and electrical resistivity are obtained for STS434L mixed with Fecralloy.

Cu-Mn과 Cu-Zn 촉매를 침전제로 다르게 하거나, 금속의 몰비율, 소성온도를 다르게 하여 공침법으로 제조하였고 CO산화반응을 수행하여 혼합산화물 촉매에서 Cu, Mn과 Zn의 영향 및 소성온 도가 미치는 영향을 조사하였다. 촉매의 물리·화학적 특성을 알아보기 위하여 XRD, N2 흡착 및 SEM 의 분석을 수행하였다. Na2CO3로 침전시켜 270℃로 소성하여 제조한 2Cu-1Mn 산화물 촉매가 저온에 서 CO 산화반응 활성이 가장 좋았으며 2Cu-1Mn 산화물 촉매는 43 m2/g으로 가장 높은 비표면적과 촉매 활성을 나타내었다. XRD로 촉매의 결정구조를 분석하였을 때 Cu0.5Mn2.5O4의 결정구조를 갖는 촉 매는 낮은 활성을 보였다. 270℃에서 소성한 촉매가 좋은 활성을 나타냈으며 Pt 촉매와 비교하여도 저 온에서 CO산화반응이 더욱 우수함을 알 수 있었다.

본 연구에서는 촉매 상 H2O2 전환에 의해 건식산화제가 생성되었으며, 이를 이용한 NO 산 화 공정에 대한 연구를 진행하였다. 건식산화제를 생성하기 위한 H2O2 촉매 전환에 관한 실험을 수행 한 결과, Mn계 촉매의 성능이 가장 우수하였으며, 이를 통해 생성된 건식산화제를 NO 산화공정에 주 입하여 다양한 운전조건에서 NO 산화특성을 조사하였다. 그 결과, H2O2 주입량, 산화반응온도, 그리고 공간속도가 NO 산화율에 크게 영향을 미치는 것을 확인하였다. 그리고, 산화반응온도와 H2O2 주입량 이 증가할수록 NO 산화효율이 증가하였으며, 공간속도가 증가할수록 NO 산화효율이 감소하였다.

The potential use of UV-TiO2 photocatalytic oxidation absorbent reactor in the removal of gaseous formaldehyde was studied. This study was conducted inside a bench-type circulation reactor chamber at ambient air conditions. PCO (Photocatalytic Oxidaion) degradation test for formaldehyde was done repeatedly and the average was reported. It was evident that photocatalytic oxidation was proven to be an effective method to control indoor air pollutants, like formaldehyde in indoor air. However, by-products are produced in the case of formaldehyde degradation also CO2, CO, H2O and formic acid are produced. These by-products can inhibit the active site of the photocatalyst. Thus, addition of adsorbent succeeding the PCO-TiO2, acts as a secondary treatment wherein produced by-products from the degradation and unreacted HCHO will adhere to the surface of the adsorbent. In this study, synthetic zeolite and activated carbon pellets were used to control of by-products of formaldehyde. PCOTiO2 degradation alone achieves 86% for a period of 60 minutes. Addition of adsorbent improves the removal efficiency achieving 90% and 96% using activated carbon pellet and zeolite, respectively.

바이오디젤은 지방산 중의 일부물질이 대기중의 산소와 결합하여 유기지방산 등을 형성하며 밀도, 동점도, 전산가, 산화안정도 등의 물성 특성에 영향을 준다. 바이오디젤의 산화안정성 문제를 해결 하기 위해 바이오디젤에 다양한 산화방지제를 첨가하여 물성 변화의 특성을 분석하였다. 첨가제의 함량 이 증가함에 따라 산화안정도는 증가하는 경향을 나타내고 대부분 첨가량에 비례적으로 증가하였다. 7 종의 첨가제 중 TBHQ가 가장 우수한 성능을 보이며 propyl gallate, butyl-amine, aniline, pyrogallol 등 4종의 첨가제도 목표치인 500 ppm 첨가 시 10시간 이상의 성능을 보였다. pyrogallol이 전산가에서 품질기준에 부적합하여 첨가제로서 적절하지 않은 것으로 나타났으며, hydroquinone계열의 TBHA, DTBHQ는 산화안정도에서 품질기준은 만족하나 연구과제의 목표치인 10 시간 이상에 미치지 못하는 결과를 보여 개발 첨가제로서는 결함이 있는 것으로 판단하였다. 또한 propyl gallate도 전산가에서 품질 기준에 적합하나 500 ppm 첨가 시 수치가 높고 첨가제 증가에 따른 전산가 증가 경향이 커서 첨가제 로서 부적합한 것으로 판단하였다.

MAO ceramic coatings were prepared on AZ61 magnesium alloy for various processing times ranging from 5 to 60 min, in an electrolyte solution based on silicate-fluoride. The mechanical, electrochemical and, microstructural properties and the phase compositions of the coating layers were investigated. In this work, unlike previous studies, coatings with high amounts of the Mag2SiO4 phase were formed which contained small amounts of MgO and MgF2 at a processing condition of 30 min. A microstructural analysis revealed that the porosity of the coatings was reduced considerably with an increase in the processing time, together with a change in the pore geometry from an irregular to a spherical shape. Potentiodynamic polarization and mechanical testing results showed that the coatings acquired after a processing time of 30 min were superior to all of the others.

TiO2 nanowires were grown by thermal oxidation of TiO powder in an oxygen and nitrogen gas environment at 1000 oC. The ratio of O2 to N2 in an ambient gas was changed to investigate the effect of the gas ratio on the growth of TiO2 nanowires. The oxidation process was carried out at different O2/N2 ratios of 0/100, 25/75, 50/50 and 100/0. No nanowires were formed at O2/N2 ratios of less than 25/75. When the O2/N2 ratio was 50/50, nanowires started to form. As the gas ratio increased to 100/0, the diameter and length of the nanowires increased. The X-ray diffraction pattern showed that the nanowires were TiO2 with a rutile crystallographic structure. In the XRD pattern, no peaks from the anatase and brookite structures of TiO2 were observed. The diameter of the nanowires decreased along the growth direction, and no catalytic particles were detected at the tips of the nanowires which suggests that the nanowires were grown with a vapor-solid growth mechanism.

The GaN-powder scrap generated in the manufacturing process of LED contains significant amounts of gallium. This waste can be an important resource for gallium through recycling of scraps. In the present study, the influence of annealing temperatures on the structural properties of GaN powder was investigated when the waste was recycled through the mechanochemical oxidation process. The annealing temperature varied from 200oC to 1100oC and the changes in crystal structure and microstructure were studied. The annealed powder was characterized using various analytical tools such as TGA, XRD, SEM, and XRF. The results indicate that GaN structure was fully changed to Ga2O3 structure when annealed above 900oC for 2 h. And, as the annealing temperature increased, crystallinity and particle size were enhanced. The increase in particle size of gallium oxide was possibly promoted by powder-sintering which merged particles to larger than 50 nm.