망간은 수중에서 대체적으로 불용성이나, 지하나 지표에서 여러 가지 반응으로 인해 수중으로 용존되어 유입된다. 용존된 망간은 먹는 물에서 0.1 mg/L 이상일 경우 불쾌한 금속냄새가 나며, 0.02 mg/L 이상에서는 박테리아에 의한 이취미가 발생할 수 있다. 또한, 망간산화물이 급배수관에 피복되어 통수능을 감소시킨다. 최근 강화된 국내 먹는 물 수질 기준치는 0.05 mg/L이다. 이러한 망간 문제를 해결할 수처리 공정 연구가 필요하다. 본 연구에서는 과망간산칼륨(KMnO4)과 차아염소산 나트륨(NaOCl)을 이용하여 망간을 산화물로 변화시키고, 이를 한외여과막으로 제거한 후의 망간제거효율을 연구하였다. 특히, 두 산화제를 복합으로 사용할 때의 효과를 분석하고 실제 적용 가능성을 타진하였다.

Alumina dispersion strengthening copper(ADSC) alloy has great potential for use in many industrial applications such as contact supports, frictional break parts, electrode materials for lead wires, and spot welding with relatively high strength and good conductivity. In this study, we investigated the oxidation behavior of ADSC alloys. These alloys were fabricated in forms of plate and round type samples by surface oxidation reaction using Cu-0.8Al, Cu-0.4Al-0.4Ti, and Cu-0.6Al-0.4Ti(wt%) alloys. The alloys were oxidized at 980 oC for 1 h, 2 h, and 4 h in ambient atmosphere. The microstructure was observed with an optical microscope(OM) and a scanning electron microscope(SEM) equipped with energy-dispersive X-ray spectroscopy(EDS). Characterization of alumina was carried out using a 200 kV field-emission transmission electron microscope(TEM). As a result, various oxides including Ti were formed in the oxidation layer, in addition to γ-alumina. The thickness of the oxidation layer increased with Ti addition to the Cu-Al alloy and with the oxidation time. The corrected diffusion equation for the plate and round type samples showed different oxidation layer thickness under the same conditions. Diffusion length of the round type specimen had a value higher than that of its plate counterpart because the oxygen concentration per unit area of the round type specimen was higher than that of the plate type specimen at the same diffusiondepth.

To improve the methanol electro-oxidation in direct methanol fuel cells(DMFCs), Pt electrocatalysts embedded on porous carbon nanofibers(CNFs) were synthesized by electrospinning followed by a reduction method. To fabricate the porous CNFs, we prepared three types of porous CNFs using three different amount of a styrene-co acrylonitrile(SAN) polymer: 0.2 wt%, 0.5 wt%, and 1 wt%, respectively. A SAN polymer, which provides vacant spaces in porous CNFs, was decomposed and burn out during the carbonization. The structure and morphology of the samples were examined using field emission scanning electron microscopy and transmission electron microscopy and their surface area were measured using the Brunauer- Emmett-Teller(BET). The crystallinities and chemical compositions of the samples were examined using X-ray diffraction and X-ray photoelectron spectroscopy. The electrochemical properties on the methanol electro oxidation were characterized using cyclic voltammetry and chronoamperometry. Pt electrocatalysts embedded on porous CNFs containing 0.5 wt% SAN polymer exhibited the improved methanol oxidation and electrocatalytic stability compared to Pt/conventional CNFs and commercial Pt/ C(40 wt% Pt on Vulcan carbon, E-TEK).

Benzene was oxidized by binary oxidants composed of nitric acid and hydrogen peroxide at 80℃. The product obtained was analyzed with gas chromatograph-mass spectrometer. Eight high value compounds, 2-nitrophenol, 2-chloro-6-nitrophenol, 4-chloro-2- nitrophenol, 2-chloro-4-nitrophenol, 2,4-dinitrophenol, 4-nitrophenol, 2,6-dinitrophenol and 2-chloro-4,6-dinitro-phenol were found, which they have high contents in the range from 4.28% to 32.52%. These compounds are very widely used in organic synthesis. e.g., synthesizing dye, medicines and chemical reagents, pesticide, explosive, polymer, etc.

Extracts from Aloe vera leaves, Aloe arborescens leaves, Aloe vera callus, Portulaca oleracea and cacao (Theobroma cacao L.) bean husk (CBH) were prepared using acetone, chloroform, ethanol, hexane, and water. Solvent extracts of Aloe vera leaf had very high antioxidant activities showing IC50 values in the ranges of 0.02-0.17 mg/ mL, and had the highest total phenolic and flavonoid content among the tested samples. We hypothesized that Aloe vera leaf and CBH extracts might possess considerable in vitro anti-glycation activities. Indeed, these extracts strongly inhibited the formation of advanced glycation end-products from RNase in the presence of ribose. The chloroform extract of Aloe vera leaf showed the strongest inhibition of AGE formation (99.9%), followed by the 95% acetone extract (92.8%) at a concentration of 1 mg/mL, exhibiting higher anti-glycation activities than those of AG and rutin (73.4% and 96.1% at 1 mg/mL, respectively). The anti-glycation activity of all extracts was correlated positively with their total contents of phenolics and flavonoids. We conclude that Aloe vera leaf extracts and their constituents may be used as anti-glycation agents.

As well-known wrought stainless steel, sintered stainless steel (STS) has excellent high-temperature anticorrosion even at high temperature of 800ºC, and exhibits good corrosion resistance in air. However, when temperature increases above 900ºC, the corrosion resistance of STS begins to deteriorate and dramatically decreases. In this study, the effects of phase and composition of STS on high-temperature corrosion resistances are investigated for STS 316L, STS 304 and STS 434L above 800ºC. The morphology of the oxide layers are observed. The oxides phase and composition are identified using X-ray diffractometer and energy dispersive spectroscopy. The results demonstrate that the best corrosion resistance of STS could be improved to that of 434L. The poor corrosion resistance of the austenitic stainless steels is due to the fact that NiFe2O4 oxides forming poor adhesion between the matrix and oxide film increase the oxidation susceptibility of the material at high temperature.

The process of oxidizing polyacrylonitrile (PAN)-based carbon fibers converts them into an infusible and non-flammable state prior to carbonization. This represents one of the most important stages in determining the mechanical properties of the final carbon fibers, but the most commonly used methods, such as thermal treatment (200°C to 300°C), tend to waste a great deal of process time, money, and energy. There is therefore a need to develop more advanced oxidation methods for PAN precursor fibers. In this review, we assess the viability of electron beam, gamma-ray, ultra-violet, and plasma treatments with a view to advancing these areas of research and their industrial application.

Landfills are nettlesome sources of malodorous gases as well as methane that has the second largest radiative forcing of long residence-greenhouse gases, followed carbon dioxide. Because methane and malodorous gases are simultaneously emitted in landfills, investigation of whether or not methane and malodorous gases affect each other’s degradation is important. Amines such as monomethylamine(MMA), dimethylamine(DMA) and trimethylamine(TMA) are representative malodorous gases from landfills. In this study, the effect of amines on the bio-oxidation of methane was evaluated using a methane-oxidizing consortium where the dominant bacteria were Methylocystis spp. Amines inhibited the methane oxidation by the consortium, and the inhibition effect increased in the order of TMA > DMA > MMA. Methane oxidation rates in the consortium decreased with increasing amine/methane ratio(mol/mol). These results can be used to design and optimize the biological processes for simultaneous removal of methane and malodorous gases.

Methanol was directly produced by the partial oxidation of methane with four-component mixed oxide catalysts. Four-component(Mo-Bi-Cr-Si) mixed oxide catalysts were prepared by the co-precipitation and sol-gel methods. The catalyst prepared by the sol-gel method showed about eleven times higher surface area than that prepared by the co-precipitation method. From the O2-TPD experiment of the prepared catalysts, it was proven that there exists two types of oxygen species, and the oxygen species that participates in the partial oxidation reaction is the lattice oxygen desorbing around 750℃. The optimum reaction condition for methanol production was 420°C, 50 bar, flow rate of 115 mL/min, and CH4/O2 ratio of 10/1.5, providing methane conversion and methanol selectivity of 3.2 and 26.7%, respectively.

Cu2O nanowires were synthesized at large scale on copper plate by thermal oxidation in air. The effect of oxidation time and temperature on the morphology of the nanowires was examined. The oxidation time had no effect on the diameter of the nanowires, while it had a great effect on the density and the length of the nanowires. The density and the length of the nanowires increased, and then decreased, with increasing oxidation time. The oxidation temperature had a tremendous effect on the size-distribution as well as the density of the nanowires. When the oxidation temperature was 700˚C, uniform size-distribution and high density of the nanowires was achieved. At lower and higher temperatures, the density of the nanowires was lower, and they displayed a broader size-distribution. It is suggested that the Cu2O nanowires were grown via a vapor-solid mechanism because no catalyst particles were observed at the tips of the nanowires.

This study was performed to obtain high conversion efficiency of NH3 and minimize generation of nitrogen oxides using metal-supported catalyst with Ag : Cu ratio. Through structural analysis of the prepared catalyst with Ag : Cu ratio ((10-x)Ag–xCu (0≤ x ≤6)), it was confirmed that the specific surface area was decrease with increasing metal content. A prepared catalysts showed Type Ⅱ adsorption isotherms regardless of the ratio Ag : Cu of metal content, and crystalline phase of Ag2O, CuO and CuAl2O was observed by XRD analysis. In the low temperature(150∼200 ℃), a conversion efficiency of AC_10 recorded the highest(98%), whereas AC_5 (Ag : Cu = 5 : 5) also showed good conversion efficiency(93.8%). However, in the high temperature range, the amounts of by-products(NO, NO2) formed with AC_5 was lower than that of AC_10. From these results, It is concluded that AC_5 is more environmentally and economically suitable.

The effect of oxygen pressure on the synthesis of ZnO nanowires by means of melt-oxidation of an Al-Zn mixture was investigated. The samples were prepared in oxygen ambient for 1 h at 1,000˚C under oxygen pressure ranging from 0.5 to 100 Torr. ZnO nanowires were formed at oxygen pressures lower than 10 Torr. As the oxygen pressure increased from 0.5 to 10 Torr, the width of the nanowires increased, but their length decreased. The ZnO nanowires had a needle shape, which became gradually thinner toward the tip. X-ray diffraction patterns showed that the nanowires had a hexagonal wurtzite structure. However, ZnO nanowires were not observed when the oxygen pressure increased from 10 Torr to 100 Torr. In roomtemperature cathodeluminescence spectra of the ZnO nanowires, the intensity of ultra-violet emission at 380 nm increased with decreasing oxygen pressure, which indicated that the lower the oxygen pressure, the better the crystallinity of the ZnO nanowires.

Fabrication of reaction-bonded Al2O3 (RBAO) ceramics using Al-Zn-Mg alloy powder was studied in order to improve traditional RBAO ceramic processing using Al powder. The influence on reaction-bonding and microstructure, as well as on physical and mechanical properties, of the particulate characteristics of the Al2O3-Al alloy powder mixtures after milling, was revealed. Variation of the particulate characteristics of this Al2O3-Al alloy powder mixture with milling time was reported previously. To start, the Al2O3-Al alloy powder mixture was milled, reaction-bonded, post-sintered, and characterized. During reaction-bonding of the Al2O3-Al alloy powder mixture compacts, oxidation of the Al alloy took place in two stages, that is, there was solid- and liquid-state oxidation of the Al alloy. The solid-state oxidation exhibited strong dependence on the density of surface defects on the Al-alloy particles formed during milling. Higher milling efficiency resulted in less participation of the Al alloy in reaction-bonding. This was because of its consumption by chemical reactions during milling, and subsequent powder handling, and could be rather harmful in the case of over-milling. In contrast to very little dependence of oxidation of the Al alloy on its particle size after milling, the relative density, microstructure, and flexural strength were strongly dependent on particle size after milling (i.e., on milling efficiency). The relative density and 4-point flexural strength of the RBAO ceramics in this study were ~98% and ~365 MPa, respectively, after post-sintering at 1,600˚C.

Odorous compounds produced from blackwater commonly cause domestic nuisance complaints. In this study, aseries of experiments was conducted to apply an electrolytic oxidation system to abate the odor problems fromblackwater. The electrolytic process removes odorous compounds from the liquid sources using direct and indirectoxidation; therefore, the system performance mainly relies on electrode materials. Four different electrodematerials, SS304, SS316, Ti, Ti/IrO₂, were applied, and the electrolytic oxidation showed that hydrogen sulfideand organic constituents were effectively removed. However, the weights of electrodes, SS304 and SS316, weredecreased by 7.5~8% due to the electrochemical decomposition from the anode surface. In order to improve thedurability and economical feasibility, SS304 was used as the cathode while Ti/IrO₂ was used as the anode. Theelectrode combination with the different materials (Ti/IrO₂:SS304) showed the same odor removal efficiency asthat using the same material (Ti/IrO₂:Ti/IrO₂). Consequentially, the electrolytic reaction to oxidize odorous andorganic constituents in humane manure was strongly affected by the electrode materials, and its combination needsto be carefully selected to achieve better performance.

The objective of this study is to investigate partial oxidation of NO with desulfurization in dry sorbent injection(DSI) process using dry sorbent and additives. The effect of the main operating variables directly related to desulfurization efficiency has been also tested. These variables are Ca/S ratio, temperature, inlet SO2 concentration and gas flow rate. The experiment was carried out for partial oxidation of NO with desulfurization in dry sorbent injection process using NaClO2 and CaCl2. The experimental results showed that partial oxidation of NO with desulfurization was increased in DSI process using little NaClO2. It was also found that the injection of CaCl2 was effective in increasing only SO2 removal efficiency. Increase of SO2 removal performance and promotion of partial oxidation of NO using the two additives at low temperature was confirmed.

Fe-Cr-Al powder porous metal was manufactured by using new electro-spray process. First, ultra-finefecralloy powders were produced by using the submerged electric wire explosion process. Evenly distributed colloid(0.05~0.5% powders) was dispersed on Polyurethane foam through the electro-spray process. And then degreasing andsintering processes were conduced. In order to examine the effect of cell size (200 µm, 450 µm, 500 µm) in process,pre-samples were sintered for two hours at temperature of 1450˚C, in H₂ atmospheres. A 24-hour thermo gravimetricanalysis test was conducted at 1000˚C in a 79% N₂ + 21% O₂ to investigate the high temperature oxidation behavior ofpowder porous metal. The results of the high temperature oxidation tests showed that oxidation resistance increased withincreasing cell size. In the 200 µm porous metal with a thinner strut and larger specific surface area, the depletion ofthe stabilizing elements such as Al and Cr occurred more quickly during the high-temperature oxidation compared withthe 450, 500 µm porous metals.

바이오디젤은 세계 화석연료의 흐름을 변화시킬 수 있는 환경 친화적 대체물질로 관심의 대상이 되고 있으며 대체연료 외에도 다양한 분야에서 수많은 응용 연구가 진행되고 있다. 최근에는 원유의 정제로부터 얻어진 석유제품을 대체하려는 다양한 움직임이 활발하게 진행되고 있다. 그 중 윤활기유로서의 식물성 오일은 급속도로 발전된 석유산업으로 인해 상용화 되지 못했던 오일로 관심의 대상이 되고 있으며 자연친화적 생분해성과 무독성, 윤활유로서의 낮은 휘발성과 우수한 계면윤활 등 대체 오일로써 충분한 가능성을 지니고 있다. 하지만 우수한 윤활 및 마모성능에도 불구하고 윤활연구에 넓게 활용되지 못했던 이유 중에는 지방산메틸에스테르가 갖는 열악한 산화안정성(oxidation stability) 및 열화안정도(thermal stability) 때문으로 보고되고 있다. 따라서 바이오디젤을 윤활기유 내 일정비율로 혼합하여 윤활성능 및 산화안정성의 변화를 확인하였으며 사구식 내마모 성능시험 후 발생되는 산화 및 열화현상을 알아보았다. 또한 산화에 따른 혼합 오일의 윤활특성 변화를 분석하였으며 이러한 결과를 바탕으로 윤활유 또는 윤활 향상제로서의 가능성을 살펴보았다.

최근 바이오디젤의 보급 활성화에 정책에 따라 석유제품에 바이오디젤 혼합량이 증가되고 있으며, 이러한 혼합량 증가에 따른 겨울철 저온특성과 산화안정성에 대한 문제가 제기되고 있다. 따라서 본 연구에서는 바이오디젤 혼합연료에 대하여 실제 저장환경을 모사하고, 저장 중 품질변화를 평가하여 저장환경별 산화 경향과 품질에 미치는 영향 등의 규명을 통해 산화 제품의 품질관리 방안을 제시하였다. 바이오디젤 혼합연료의 산화열화 평가 결과, 직접적인 햇빛 노출 및 대기노출이 없는 저장용기에서는 여름철 약 18주간은 산화에 의한 특별한 품질저하는 없었지만, PE 재질 플라스틱 용기의 경우 약 2주간의 햇빛노출에 급격한 산화가 일어나 품질저하를 초래하였다. 이러한 현상을 일부 품질변화뿐만 아니라 FT-IR 스펙트럼 변화로도 확인 할수 있었다. 하지만 산화가 상당히 진행된 연료라도 품질기준을 모두 만족하여 품질검사 항목만으로는 특별한 현상을 발견할 수 없었다. 즉, 품질기준을 만족하더라도 산화로 인한 산화 생성물(고분자물질, 유기산 등)에 의해 차량 문제를 유발할 수 있는 충분한 여지가 있었다.

페롭스카이트 촉매와 Mo, Bi를 기본으로 하는 복합 산화물 촉매를 이용하여 천연가스의 주성분인 메탄의 부분산화를 통하여 메탄올을 직접 합성하였다. 페롭스카이트(ABO₃) 촉매는 A 및 B site 성분을 변화시키면서 사과산법으로 제조하였으며, Mo, Bi를 기본으로 하는 3성분계 복합 산화물 촉매는 공침법으로 제조하여 반응특성을 살펴보았다. 페롭스카이트 촉매에서 A site에 알칼리 금속인 Sr을, B site에 전이금속인 Cr을 도입한 SrCrO₃ 촉매가 400℃에서 메탄올 선택도 11%로 가장 우수한 결과를 보였다. Mo, Bi를 기본으로 하는 3성분계 복합 산화물 촉매의 경우 모든 촉매에서 메탄 전환율에는 큰 차이를 보이지 않았으며, Cr을 첨가한 Mo-Bi-Cr 복합 산화물 촉매가 400℃에서 메탄올 선택도 15.3% 로 가장 우수한 결과를 나타냈다. 3성분계 복합 산화물 촉매에서 촉매의 활성과 메탄올 선택도는 촉매의 표면적에 정비례하였다.

In this study, analysis on the oxidation behavior was conducted by a series of high-temperature oxidation tests at both 800oC, 900oC and 1000 in the air with sintered STS 316L. The weight gain of each oxidized specimen was measured, the oxidized surface morphologies and composition of oxidation layer were analyzed with Scanning Electron Microscope-Energy Dispersive x-ray Spectroscopy (SEM-EDS), finally, the phase change and composition of the oxidized specimen were shown by X-Ray Diffraction (XRD). As a result, the weight gain increased sharply at 1000oC when oxidation test was conducted for 210 hours. Also, a plentiful of pores were observed in the surface oxidation layers at 900oC for 210 hours. In addition, the following conclusions on oxidation behavior of sintered STS 316L can be obtained: Cr2O3 can be formed on pores by influxing oxygen through open-pores, (Fe0.6Cr0.4)2O3 can be generated on the inner oxidation layer, and Fe2O3 was on the outer oxidation layer. Also, NiFe2O4 could be precipitated if the oxidation time was kept longer.