Methanol and formaldehyde were produced directly by the partial oxidation of methane. The catalysts used were mixed oxides of late-transition metals, such as Mn, Fe, Co, Ni and Cu. The reaction was carried out at 450℃, 50 bar in a fixed-bed differential reactor. The prepared catalysts were characterized by XRD, TPD and BET apparatus. Of the catalysts, A-Mn0.2-6, which contains 0.2 mole of Mn and calcined at 600℃, showed the best catalytic activity: 3.7% methane conversion, and 30 and 28% methanol and formaldehyde selectivities, respectively. The catalytic activity was changed with the content of Mn and the calcination temperature. Catalytic activity increased with the specific surface areas of the catalysts. With XRD, it was found that the structure of the catalysts are changed with calcination temperature. Through O2-TPD experiment, it was found that the catalysts showing good catalytic activity showed O2 desorption peak around 800℃.

Seasoning oil(SO-1) was manufactured from soybean oil, with β-carotene, oleoresin paprika and 3 kinds of flavors. Color of it's SO-1 was red. Total content of trans fatty acid of SO-1 was low level 0.84%, compare to the butter's and margarine's 1.35%, 28.31%, respectively. Total volatile components of SO-1 was 201,313.11ppm, was higher than soybean oil's, butter's, margarine's and SO-2's(removed 3 kinds of flavors from SO-1), it's value of 63.54ppm, 481.24ppm, 168.95ppm and 205.73ppm, respectively. And smoke point(SP) of SO-1 was higher than others. SP of SO-1, after 6 months later at room temperature, was 240, in contrast with soybean oil's 228. This SO-1, added β-carotene and flavor components, had a masking effect of burnt flavor. From these results, SO-1 can be replaced of butter or margarine as a substituted oil.

조사후 핵연료 가열(PIA장비)를 이용한 고연소도 UO2 사용후 핵연료의 산화 및 가열후 미세조직의 변화를 관찰하였다. 울진 2호기에서 한국원자력연구소 조사후시험시설로 이송된 국산 경수로용 고연소도 사용후 핵연료는 봉평균 연소도가 57,000 MWd/tU-rod avg.이였다. 본 시험에 사용된 시편은 국부연소도 65,000 MWd/tU UO2 소결체의 고형체 200 mg을 사용하였다. 본 시편을 사용후 핵 연료 가열(PIA) 시험장비를 이용하여 핫셀 내에서 3시간의 산화시험과 연속적으로 까지 가열하였다. 결정립경계까지의 산화를 위하여 에서 헬륨 50 ml, 표준공기 100 ml를 흔합한 산화분위기로 3시간을 유지하였다. 핵분열기체 방출거동을 알기위해 시험 전과정중에 85Kr의 방출량을 베타 측정기와 감마 측정기를 이용하여 실시간으로 측정 하였다. 가열시험이 종료된 후 전자주사현미경을 이용하여 미세구조의 변화를 관찰하였다. 시험결과 가열하는 동안 핵분열생성물은 UO2기지의 결정립경계와 표면으로 이동된 것을 관찰하였다. 이 시편은 환원과정을 통하여 재구조화 되었고, 정도의 결정립크기를 가진 것으로 나타났다.

This study was aimed to investigate treatment feasibility of leachate from D landfill that is located in gyr대ungbuk. From the analytical results of leachate, organic and nonbiodegradable matters were contained in high concentration. Thus chemical treatment was introduced to degrade nonbiodegradable matters in pre or post biological process. Two types of Fenton oxidation were adapted in this study. The first one is pre treatment process before biological treatment. The second one is post treatment process after biological treatment. The optimal conditions of both treatment methods were investigated as follows. In case of pre treatment process, the optimal conditions appeared in Fe+2/H2O2(mmol/mmol): 0.1, H2O2/CODcr(mg/mg): 27.0, pH: 3 and reaction time: 2hrs. On the other hand, in case of post treatment process, the optimal conditions appeared in Fe2+(mmol/mmol): 0.14, H2O2/CODcr(mg/mg): 57.4, pH: 3 and reaction time: 1.25hrs. In the above optimal conditions, high COD removal was obtained in pre and post treatment process. Also it can expect that Fenton oxidation converted nonbiodegradable matters into biodegradable matters.

원전에서 발생된 농축폐액 방사성폐기물로부터 및 를 분리 정량하기 위하여 potassium persulfate와 sulfuric acid의 산화제를 이용하는 산화증류법을 적용하였으며, 와 는 각각 기체와 HTO 액체로 순차적으로 분리되었다. 분리된 와 는 액체섬광계수기를 이용하여 계수되었고, 소광효과를 보정하여 방사능을 측정하였다. 산화증류법을 검증하기 위하여 방사성 표준물은 와 , 그리고 의 3종류, 그리고 방사성 표준물은 HTO가 이용되었다. 또한 산화되기 어려운 방향족 화합물 중 을 대상으로 가장 최적의 산화 조건을 조사하고자 황산용액 농도에 따라 FT-IR 피크 변화를 평가하였다. 방사성표준시료의 경우와 동일한 방법으로 원전 농축폐액 시료로부터 와 를 분리 검출하였는데, 그 결과 회수율은 와 가 각각 Bq/g와 Bq/g로 검출되었다.

Anti-oxidation coatings are the key technique for carbon/carbon (C/C) composites used as the thermal structural materials. The microstructure and oxidation behavior of several kinds of high-performance ceramic coatings for C/C composites prepared in Northwestern Polytechnical University were introduced in this paper. It showed that the ceramic coatings such as SiC, Si-MoSi2, SiC-MoSi2, Al2O3-mullite-SiC and SiC/yttrium silicate/glass coatings possessed excellent oxidation resistance at high temperatures, and some of these coatings were characterized with excellent thermal shock resistance. The SiC-MoSi2 coating system has the best oxidation protective property, which can effectively protect C/C composites from oxidation up to 1973 K. In addition, the protection and failure reasons of some coatings at high temperature were also provided.

This paper presents applicability of Fenton oxidation to perchloroethylene(PCE) contaminated soil. The initial concentration of PCE was 187mg/kg and Fenton oxidation conditions were 1.0M H2O2 and 0.5M Fe2+. More than 97% of PCE decomposition and 98% of dechlorination were obtained within 5 hrs. It was found that the decomposition of PCE by Fenton oxidation was followed pseudo first order and its reaction coefficient was 0.78 hr-1. GC-MS and GC-ECD analysis of reaction intermediates confirmed only the presence of trichloroacetic acid(i.e., 1.0% of initial PCE concentration). Under Fenton oxidation conditions, it was proposed that PCE was decomposed not simultaneously but one by one.

In order to prevent the oxide formation on the surface of nano-size iron particles and thereby to improve the oxidation resistance, iron nanoparticles synthesized by a chemical vapor condensation method were directly soaked in hexadecanethiol solution to coat them with a polymer layer. Oxygen content in the polymer-coated iron nanoparticles was significantly lower than that in air-passivated particles possessing iron-core/oxide-shell structure. Accordingly, oxidation resistance of the polymer-coated particles at an elevated temperature below in air was times higher than that of the air- passivated particles.

실증용 UO pellet 산화로의 실증을 위한 제한된 핫셀 공간 안에서 사용후 핵 연료를 취급하는 산화로는 소형화 하여야 하고, 사용후 핵 연료 분말은 UO pellet 산화로 장치로부터 비산되지 않아야 한다. 본 연구에서는 분말의 최종속도를 구하기 위하여 Stokes식과 밀도비식을 제안하였다. UO 의 최종속도 SiO 의 최종속도를 사용하여 예측하였고, 비산방지를 할 수 있는 최적유량을 결정하였다. SiO 의 이론 최종속도 식을 검증하고, UO 과 관계식을 예측하기 위하여 아크릴 장치를 만들었다. 목업시설 에 설치 된 산화로에서 제안된 이론최종속도식 인 Stokes식 의 20 L/min과 밀도비식의 14.5 L/min을 적용하여 UO 분말의 필터감지에 의해 검증하였다. 그 결과 밀도비식에 의한 14.5 L/min은 UO 이전혀 검출되지 않았고, Stokes식의 20 L/min에서는 평균 7m 의 입도분말이 검출되었다. 따라서 UO pellet 산화로에서 UO이 비산되지 않는 최적유량은 14.5L/min임을 알 수 있었고, 제안된 밀도비식이 바람직함을 알 수 있었다.

Isotropic pitch based carbon fibers were exposed to isothermal oxidation in carbon dioxide gas to study the activation kinetics under the temperature of 800~1100℃. The kinetic equation f=1--(-atb) was introduced and the constant b was obtained in the range of 0.92~1.25. It was shown that the activated carbon fiber shows the highly specific surface area (SSA) when the constant b comes close to 1. The activation kinetics were evaluated by the reaction-controlling regime (RCR) according to changes of the apparent activation energy with changes of the conversion. It was observed that the activation energies increase from 47.6 to 51.2 kcal/mole with the conversion increasing from 0.2 to 0.8. It was found that the pores of the activated carbon fiber under the chemical reaction were developed well through the fiber.

Methanol was synthesized by homogeneous and catalytic reactions of partial oxidation of methane. The effect of pressure, temperature and oxygen concentration on methanol synthesis was investigated. The catalyst used was Bi-Cs-Mg-Cu-Mo mixed oxide. The partial oxidation reaction was carried out in a fixed bed reactor at 20~46 bar and 450~480℃ and oxygen concentration of 5.3~7.7mol%. The results were compared with results of homogeneous reaction performed at the same conditions. Methane conversions of the homogeneous and catalytic reactions increased with temperature. Methanol selectivity of the homogeneous reaction decreased with increasing temperature. However, the methanol selectivity of catalytic reaction increased with temperature. For both homogeneous and catalytic reactions, the methane conversions were around 5%. This may be due to the low oxygen concentration. Methanol selectivity of the catalytic reaction was higher than that of homogeneous one.

사용후핵연료 금속전환체의 저장 안정성을 높이기 위해 금속전환체의 주성분인 금속우라늄과 산화 안정화물질로 알려져 있는 Nb을 첨가하여 모의 금속전환체 합금을 제작하였다. 모의 금속전환체 합금을 온도구간에서 순수 산소분위기로 산화시험을 수행하고 무게증가를 열중량 분석기(TGA)로 측정하였다. 산화 실험결과 U-Nb 모의 금속전환체는 순수 금속우라늄에 비하여 상당한 산화 저항성을 가졌다. U-Nb 합금의 경우 Nb의 함량 에 따라 각각 온도가 일 경우에는 1.61, 7.78, 11.76, 20.14배 , 에서 1.45, 5.98, 10.08, 11.15배, 에서 1.33, 4.82, 8.87, 6.84배 순수 금속우라늄에 비해 산화저항성이 향상되는 것으로 나타났다. 또한 Nb 합금에 대한 활성화에너지는 kcal/mol 로 나타났다.

Chop molding composites and 2D carbon/carbon composites were manufactured by hot press molding method. Phenol resin of novolac type was used for matrix precursor and PAN-based carbon, PAN-based graphite and pitch-based carbon fiber were used for reinforcement and boron oxide was used for oxidation retardant. All of the composites were treated by 2000℃ and 2400℃ graphitization process, respectively. After graphitization process, amount of a boron residue in carbon/carbon composites is much according to irregularity of used raw materials. Under the presence of boron in carbon/carbon composites, catalytic effect of boron was a little at 2000℃ graphitization temperature. However, it was quite at 2400℃ graphitization.