염화철(Ferrous Choloride) 증기의 고온 수소환원 반응을 통한 미립질 철분말의 생성속도에 대한 이론적인 해석돠 실험을 수행하였다. 철분말의 생성기구는 염화철이 증발하여 생성된 증기와 운반가스인 알곤을 혼합하여 반응부로 유입시키고 수소에 의한 고온환원반을을 통하여 철분말과 함께 부산물인 염화수소(HCI) 가스를 얻게 된다. 생성된 반응부 후미에 설치한 유기용매 포집기를 이용하여 회수하였으며, 염화수소는 가성소다 수용액에 흡수시키고 이를 적정함으로써 초기 반응물인 염화철의 전환율을 계산하였다. 반응속도식의 반응물에 대하여 1차반응(1st-order reaction)이고 염화철 증가와 운반체인 알곤가스가 평형상태일 때의 속도상수는 k=7,879exp(-53,840/RT)dm3/mole.sec으로 표시되며, 이때의 활성화에너지는 53.84kJ/mole이었다. 철분말의 TEM 사진에 의하면 입도범위는 0.1~1.0μm이며, 반응온도 및 가스유량에는 크게 영향을 받지 않는것으로 나타났다.

The microstructure evolution during sintering of a compact being composed of three layers of (WC-15%Co)/Fe powder mixture with different Fe contents has been observed. The Fe contents in the respective (WC-15%Co)/Fe layers were varied by 20%. 50%, and 90% in sequence by volume from a top layer to a bot- tom layer. The sintering temperatures and times were varied from 110 to 125 and from 1 h to 4 h, The compact layer was not densified below 120 in 4 h. Appropriate sintering temperature and time conditions for making a multi-layered hard metal compact were determined as 125 and 3 h, respectively.

The compacts of pure and phosphorus-coated iron powder with 0~0.8%C were sintered at for 40 min. in cracked ammonia gas atmosphere. The tensile and impact strengths were measured and the relationship of the results with carbon content, phosphorus, quenching and tempering was investigated. The results obtained can be summarized as follows : (1) The tensile strength of sintered compacts increased slowly with carbon content. Increase in tensile strength by heat treatment was evident especially in the low carbon specimen. The specimen with phosphorus showed higher strength compared to pure iron compacts value. (2) No inflection point of elasticplastic deformation on stress-strain curve was observed in sintered steel. The elastic modulus of sintered steel had the same tendency as tensile strength. But the elongation showed the opposite tendency. (3) The impact absorption energy of sintered steel without addition of phosphorus decreased successively with carbon content and by quenching and tempering. On the contrary, addition of phosphorus resulted in an increase of the impact absorption energy. Quenching and tempering did not affect the impact energy especially in high carbon content. (4) The main fracture source was pore in specimen and the propagation of crack occured mostly along the grain boundaries. But the intragranular fracture was also observed in high carbon, quenched and tempered specimen, and especially in the specimen with phosphorus.

When a commercial prealloyed Fe-powder(Fe-5Cr-lMo-2Cu-0.5P-3C) is liquid phase sintered at 116, liquid precipitates with various shapes form within solid grains during the initial stage of sintering. The shape of a liquid precipitate changes pith the increment of their size from sphere(with radius<0.3), a transient polyhedron with more than 7 faces(1~2 ), cuboid(3~5 ), and finally to sphere(>5 ). The shapes of liquid precipitates closely resemble the growth shapes predicted on the basis of solid-liquid interfacial energy and the coherency strain energy with anisotropic elastic constants in the diffusion zone around the precipitates.

Commercial pure iron powder and iron powder of coated 0.45% phosphorus were mixed with graphite powder in dry mixer to control carbon content from 0 wt% to 0.8 wt%. Mixed powder was pressed in the mould under the pressure of 510 MPa. Compacts were sintered at 118 for 40 min. in cracked ammonia gaseous atmosphere. Some of these sintered specimens were quenched in oil, and tempered in Ar gas. All of these specimens were investigated for microstructure, density and hardness in relation to coated phosphorus and carbon content. The results obtained were as follows: (1) The microstructure of the sintered speciments revealed that the amount of pearlite was increased with increasing C content but decreased by P-addition. (2) The P-addition affected the microstructure of pores in which the pore shape became round and its mean size was decreased by P-addition. (3) After tempering of sintered specimens the structure of pearlite was changed from fine structure to coarse one in P added specimen. (4) Hardness was higher in P added specimens.

시약급 망간염과 폐건전지에서 회수한 망간염 수용액을 전해액으로 사용하고, 0.2% 저탄소 연강을 가용성 양극으로, SUS 304 스테인레스 강을 음극으로 하여 전기분해 법에 의해 생성된 망간 페라이트의 화학조성 및 열적, 자기적 성질을 조사한 결과 다음과 같다. MnxFe3-xO4(O<X<3) 산화물은 X=1에서 스핀넬형 망간 페라이트가 생성되었고, 망간함량이 증가할수록 200˚C까지는 중량감소량이 직선적으로 증가하였다. 망간함량과 가열온도가 증가할수록 보자력이 감소하고 포화자화도 감소하는 경향을 보였다. 시약급 염화망간염을 전해액으로하여 생성시킨 망간 페라이트가 황산망간 및 폐건전지에서 회수한 망간염을 전해액으로 사용하여 제조한 망간 페라이트 보다 포화자화값이 높았다. 200˚C, 300˚C로 가열하였을 때, 폐건전지에서 침출한 황산망간염을 전해액으로 하여 생성시킨 망간 페라이트가 시약급 황산망간염을 전해액으로 하여 생성시킨 망간 페라이트 보다 포화자화와 잔류자화값이 높았다. 생성된 입도는 모두 구형이었고, 시약급 황산망간염을 전해액으로 하여 생성시킨 망간 페라이트에서는 0.1μm, 폐건전지에서 침출한 황산망간염을 전해액으로 하여 생성시킨 망간 페라이트에서는 0.5μm 범위의 미립자로 생성되었다.

The advanced oxidation treatment using persulfate and zero-valent iron (ZVI) has been evaluated as a very effective technology for remediation of soil and groundwater contamination. However, the high rate of the initial reaction of persulfate with ZVI causes over-consumption of an injected persulfate, and the excessively generated active species show a low transfer rate to the target pollutant. In this study, ZVI was modified using selenium with very low reactivity in the water environment with the aim of controlling the persulfate activation rate by controlling the reactivity of ZVI. Selenium-modified ZVI (Se/ZVI) was confirmed to have a selenium coating on the surface through SEM/EDS analysis, and low reductive reactivity to trichlroethylene (TCE) was observed. As a result of inducing the persulfate activation using the synthesized Se/ZVI, the persulfated consumption rate was greatly reduced, and the decomposition rate of the model contaminant, anisole, was also reduced in proportion. However, the final decomposition efficiency was rather increased, which seems to be the result of preventing persulfate over-consumption. This is because the transfer efficiency of the active species (SO4-∙) of persulfate to the target contaminant has been improved. Selenium on the surface of Se/ZVI was not significantly dissolved even under oxidation conditions by persulfate, and most of it was present in the form of Se/ZVI. It was confirmed that the persulfate activation rate could be controlled by controlling the reactivity of ZVI, which could greatly contribute to the improvement of the persulfate oxidation efficiency.

본 연구는 철계-형상기억합금을 통해 구조물에 프리스트레스 부여하기 위한 기초 연구로써 철계-형상기억합금-모르타르 복합체의 합성거동을 평가하였다. 실험 변수로 철계-형상기억합금의 활성화 온도를 100 ~ 190℃까지 30℃ 간격으로 설정하였다. 실험 결과 철계-형상기억합금의 활성화 온도가 30℃ 증가함에 따라 철계-형상기억합금-모르타르 복합체의 회복응력은 약 30% 증가하는 경향을 나타내었다. 그러나 활성화 온도가 190℃인 실험체는 모르타르에 균열을 발생시킨다.

Arsenic is among the heavy metals commonly found in aqueous environments. Iron oxide is known as an efficient adsorbent for the arsenic. A new synthetic method was applied to provide iron oxide giving a large specific surface area. The mixing method affects the formation of iron oxide. Ultrasonic waves assisted the formation of very fine iron oxide in an organic phase. The synthesized iron oxide is amorphous type with a high surface area of more than 181.3 m2/g. Sorption capacity of the synthesized adsorbent was relatively very high for arsenic and varied depending on the oxidation state of arsenic: a higher capacity was obtained with As(V). Lower solution pH provided a higher sorption capacity for As(V). The competitive effect of co-exist anions such as chloride, nitrate, and sulfate was minimal in sorption capacity of the iron oxide for arsenic.