• Elastomers and Composites
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• 제38권1호
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• pp.81-87
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• 2003

본 연구에서는 $FeCl_2{\cdot}4H_2O,\;(CH_2)_6N_4$ (hexamethylene tetramine) 그리고 $NaNO_2$로부터 $Fe_3O_4$ (magnetite)를 제조하고 결정성 CR고무에 배합하여 전도성 충전제의 함량이 물성에 미치는 효과와 전기전도도 (${\sigma}$)의 온도 의존성을 조사하였다. 최소 최적 혼합비(percolation threshold, $P_c$) 개념이 본 연구에서 제조한 전도성 입자가 충전된 복합체에 적용되며, 혼합물내 $Fe_3O_4$의 분율이 27%를 초과할 때 전기전도도가 급격히 증가함을 확인하였다. 전기전도도의 온도 의존성은 $P_c$ 또는 그 이하에서 열적으로 활성화되며 magnetite가 CR 고무의 강화 및 전도성 충전제로서의 역할을 할 수 있음을 조사하였다. 또한, 50 phr의 magnetite가 충전된 복합체가 최적의 물리적 가교점으로 인하여 가장 우수한 인장강도와 파단시 신장율을 보였으며 모듈러스가 magnetite 의 강화효과 및 블랜드물의 가황 토오크 곡선으로부터 얻은 점도와 관련이 있음을 확인하였다.

• 접착 및 계면
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• 제14권2호
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• pp.82-87
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• 2013

본 연구에서는 레졸, 질산철 그리고 트리블럭 공중합체를 이용하여 직접 탄화과정에 의해 자성체 나노입자가 분산된 탄소나노세공체를 합성하였다. 나노세공 마그네타이트/카본($Fe_3O_4$/carbon) 나노복합체는 낮은 마그네타이트 함량(1 wt%)을 가지고 잘 배열된 이차원적 육방체 구조(p6mm)를 보이며, 균일한 세공크기(3.6 nm), 높은 표면적(635 $m^2/g$)과 세공부피(0.48 $cm^3/g$)를 가진다. 작은 입자크기(10.2 nm)를 가지는 마그네타이트 나노입자는 초상자기성(7.7 emu/g)을 보이고 탄소 세공벽 내에 잘 분산되었다. 나노세공 마그네타이트/카본 물질은 최대 995 mg/g의 아이부프로펜 흡착량을 보였다. 또한, 자석을 이용하여 용액과 나노세공 마그네타이트/카본 물질의 분리가 용이하였다. 본 연구에서 제조된 나노복합체는 우수한 아이부프로펜 흡착제로 작용하였다.

• 자원리싸이클링
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• 제9권5호
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• pp.33-37
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• 2000

• 한국자기학회:학술대회 개요집
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• 한국자기학회 1994년도 추계연구발표회 논문개요집
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• pp.84-85
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• 1994

• 한국자기학회:학술대회 개요집
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• 한국자기학회 2001년도 춘계연구발표회 논문개요집
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• pp.118-119
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• 2001

• 한국지하수토양환경학회지:지하수토양환경
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• 제21권6호
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• pp.14-21
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• 2016

This study evaluated the applicability of stabilization of arsenic (As)-contaminated soil with iron (Fe) oxides at the former Janghang smelter site. Three Fe oxides (magnetite, goethite, and hematite) were tested as stabilizing agents to one soil sample collected from the study site. Amendment of 5% of magnetite, goethite, or hematite for one week showed the 64, 58, and 36% of reduction of the SBRC (Solubility/Bioavailability Research Consortium)-extractable (bioaccessible) As, respectively. Duration of stabilization more than one week did not show an additional reduction in SBRC-extractable As. Amendment of 5% of magnetite, which showed the highest As stabilization efficiency, was applied to 24 soil samples collected from the same site for one week, and 72% of reduction in the bioaccessible As was observed. The potential carcinogenic human health risk at the study site caused by As was $1.7{\times}10^{-5}$, which could be reduced to $8.1{\times}10^{-6}$ by the amendment of 5% magnetite for one week.

• Advances in environmental research
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• 제4권2호
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• pp.69-81
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• 2015

A new magnetite-silica core/shell nanocomposite ($Fe_3O4@nSiO_2@mSiO_2$) was synthesized and functionalized with trimethylchlorosilane (TMCS). The prepared nanocomposite was used for the removal of diesel oil from aqueous media. The characterization of magnetite-silica nanocomposite was studied by X-ray diffraction (XRD), Fourier transform infrared (FTIR), transmission electron microscopy (TEM), surface area measurement, and vibrating sample magnetization (VSM). Results have shown that the desired structure was obtained and surface modification was successfully carried out. FTIR analysis has confirmed the presence of TMCS on the surface of magnetite silica nanocomposites. The low- angle XRD pattern of nanocomposites indicated the mesoscopic structure of silica shell. Furthermore, TEM results have shown the core/shell structure with porous silica shell. Adsorption kinetic studies indicated that the nanocomposite was able to remove 80% of the oil contaminant during 2 h and fit well with the pseudo-second order model. Equilibrium studies at room temperature showed that the experimental data fitted well with Freundlich isotherm. The magnetic property of nanocomposite facilitated the separation of solid phase from aqueous solution.

• Bulletin of the Korean Chemical Society
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• 제23권11호
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• pp.1513-1518
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• 2002

Kinetic studies on the water-gas shift reaction catalyzed by magnetite/chromium oxide and copper/zinc oxide were carried out by using an in situ photoacoustic spectroscopic technique. The reactions were performed in a closed-circulation reactor system using a differential photoacoustic cell at total pressure of 40 Torr in the temperature range of 100 to $350^{\circ}C.$ The CO2 photoacoustic signal varying with the concentration of CO2 during the catalytic reaction was recorded as a function of time. The time-resolved photoacoustic spectra obtained for the initial reaction stage provided precise data of CO2 formation rate. The apparent activation energies determined from the initial rates were 74.7 kJ/mol for the magnetite/chromium oxide catalyst and 50.9 kJ/mol for the copper/zinc oxide catalyst. To determine the reaction orders, partial pressures of CO(g) and H2O(g) in the reaction mixture were varied at a constant total pressure of 40 Torr with N2 buffer gas. For the magnetite/chromium oxide catalyst, the reaction orders with respect to CO and H2O were determined to be 0.93 and 0.18, respectively. For the copper/zinc oxide catalyst, the reaction orders with respect to CO and H2O were determined to be 0.79 and 0, respectively.

• Nuclear Engineering and Technology
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• 제44권8호
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• pp.945-952
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• 2012

The sorption of selenium ions onto iron and iron compounds as a disposal container material and its corrosion products, and onto bentonite as a buffer material, was studied to understand the behaviors of selenium in a waste repository. Selenite was sorbed onto commercial magnetite very well in solutions at around pH 9, but silicate hindered their sorption onto both magnetite and ferrite. Unlike commercial magnetite and ferrite, flesh synthesized magnetite, green rust and iron greatly decreased selenium concentration even in a silicate solution. These results might be due to the formation of precipitates, or the sorption of selenide or selenite onto an iron surface at below Eh= -0.2 V. Red-colored Se(cr) was observed on the surface of a reaction bottle containing iron powder added into a selenite solution. Silicate influences on the sorption onto magnetite and iron for selenide are the same as those for selenite. Even though bentonite adsorbed a slight amount of selenite, the sorption cannot be ignored in the waste repository since a very large quantity of bentonite is used.

• 자원환경지질
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• 제29권1호
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• pp.11-21
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• 1996

The first Mg-skarn minerals are found from magnetite ore deposits of the Janggun mine, Korea. The skarn minerals are composed of mostly chondrodite, olivine， chlorite, serpentine, phlogophite, talc, apatite, magnesite， dolomite, siderite and trace amount of clinopyroxene, amphibole, garnet, wollastonite associated with magnetite, pyrrhotite and pyrite. The skarn zone is developed in the magnetite deposits at the contact of the Mg-rich Janggun Limestone Formation and the Chunyang granite. The chondrodites are columnar and radial shapes and some of them show twins. The chemical compositions of twinning-type chondrodites have high FeO (4.63 to 5.6 wt%), MnO (0.26 to 0.46 wt%) and low MgO (55.02 to 56.18 wt%) relative to the radial-type chondrodites. Twinning in chondrodite has been formed in close relation to substitution between Mg and Fe + Mn in humite solid solution. Temperature, $-logfo_2$ and $X_{CO2}$ during the skarn stage of magnetite deposits from the Janggun mine range from 395 to $430^{\circ}C$, from 30.5 to 31.2 atm and from 0.06 to 0.09, respectively.