• 한국세라믹학회지
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• 제32권2호
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• pp.234-238
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• 1995

MgFe2O4 formation, grain growth in Fe2O3, Fe solid-solution limit in MgO for MgO-Fe2O3 mixture were studied by means of investigating the distribution of phases and compositions in reaction area between MgO and Fe2O3. The reaction area at equlibrium was composed with MgO-FexO matrix and MgFe2O4 precipitation, MgFe2O4 was formed by precipitating from MgO-FexO matrix dependent on oxygen partial pressure. Fe contents was exponentially decreased with diffusion distance in MgO single crystal, and thus Fe solid-solution limitation in MgO was about 4mol%. The grain growth rate in Fe2O3 base was increased with Mg contents diffused from MgO single crystal.

• 한국세라믹학회지
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• 제34권7호
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• pp.738-746
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• 1997

MgO clinker and two kinds of dolomite clinkers with different microstructures and CaO contents were used as starting materials, and the effects of Fe2O3 addition on the properties of MgO and dolomite were investigated in the range of 2 to 8 wt% of Fe2O3 content. Secondary phases contributed to densification of MgO-Fe2O3 and dolomite-Fe2O3 were magnesioferrite and dicalciumferrite, respectively. Sinterabilities of MgO-Fe2O3 and dolomite-Fe2O3 were directly proportional to the amount of secondary phases. Also, sinterability of dolomite itself was dependent on the microstructure of starting material including distribution of CaO and MgO as well as the addition amount of Fe2O3. The flexural strength of MgO-Fe2O3 content was almost constant. The hydration resistance of dolomite with large size of MgO and discontinuous distribution of CaO was higher than that of dolomite with small size of MgO and continuous distribution of CaO. Also, the minimum content of Fe2O3 to prevent they hydration of dolomite was about 4wt%. As increasing Fe2O3 content, the penetration resistance of MgO-Fe2O3 was improved by the increment of magnesioferrite. On the other hand, the penetration resistance of dolomite-Fe2O3 was decreased because of the increment of dicalciumferrite having low melting point.

• Bulletin of the Korean Chemical Society
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• 제26권2호
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• pp.281-284
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• 2005

The Fe/MgO catalysts with different Fe loadings (1, 4, 6, 15 and 30 wt% Fe) were prepared by a wet impregnation with iron nitrate as precursor. All of the catalysts were characterized by BET surface analyzer, X-ray diffraction (XRD), temperature-programmed reduction (TPR), and X-ray photoelectron spectroscopy (XPS). The maximum removal capacity of $H_2S$ was obtained with 15 wt% Fe/MgO catalyst which had the highest BET surface area among the measured catalysts. XRD of Fe/MgO catalysts showed that well dispersed Fe particles could be present on Fe/MgO with Fe loadings below 15 wt%. The crystallites of bulk $\alpha$-$Fe_2O_3$ became evident on 30 wt% Fe/MgO, which were confirmed by XRD. TPR profiles showed that the reducibility of Fe/MgO was strongly related to the loaded amounts of Fe on MgO support. Therefore, the highest removal efficiency of $H_2S$ in wet oxidation could be ascribed to a good dispersion and high reducibility of Fe/MgO catalyst. XPS studies indicated that the $H_2S$ oxidation with Fe/MgO could proceed via the redox mechanism ($Fe^{3+}\;{\leftrightarrow}\;Fe^{2+}$).

• Bulletin of the Korean Chemical Society
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• 제18권8호
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• pp.831-840
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• 1997

Core/shell structured composite metal oxides of Fe2O3/MgO were prepared by thermal decomposition of Fe(acac)3 adsorbed on the surface of MgO cores. The morphology of the composites conformed to that of the MgO used as the cores. Broad powder X-ray diffraction peaks shifted toward larger d, large BET surface area (∼350 m2/g), and the size of crystalline domains in nano range (4 nm), all corroborate to the nanocrystallinity of the Fe2O3/MgO composite which was prepared by using nanocrystalline MgO as the core. By use of microcrystalline MgO as the core, microcrystalline Fe2O3/MgO composite was prepared, and it had small BET surface area of less than 35 m2/g. AFM measurements on nanocrystalline Fe2O3/MgO showed a collection of spherical aggregates (∼80 nm dia) with a very rough surface. On the contrary, microcrystalline Fe2O3/MgO was a collection of plate-like flat crystallites with a smooth surface. The nitrogen adsorption-desorption behavior indicated that microcrystalline Fe2O3/MgO was nonporous, whereas nanocrystalline Fe2O3/MgO was mesoporous. Bimodal distribution of the pore size became unimodal as the layer of Fe2O3 was applied to nanocrystalline MgO. The macropores in a wide distribution which the nanocrystalline MgO had were absent in the nanocrystalline Fe2O3/MgO. The decomposition of CCl4 was largily enhanced by the overlayer of Fe2O3 on nanocrystalline MgO making the reaction between nanocrystalline Fe2O3/MgO and CCl4 be nearly stoichiometric. The reaction products were environmentally benign MgCl2 and CO2. Such an enhancement was not attainable with the microcrystalline samples. Even for the nanocrystalline MgO, the enhancement was not attained, if not with the Fe2O3 layer. Without the layer of Fe2O3, it was observed that the nanocrystalline domain of the MgO transformed into microcrystalline one as the decomposition of CCl4 proceeded on its surface. It appeared that the layer of Fe2O3 on the particles of nanocrystalline Fe2O3/MgO blocked the transformation of the nanocrystalline domain into microcrystalline one. Therefore, in order to attain stoichiometric reaction between CCl4 and Fe2O3/MgO core/shell structured composite metal oxide, the morphology of the core MgO has to be nanocrystalline, and also the nanocrystalline domains has to be sustained until the core was exhausted into MgCl2.

• 한국재료학회지
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• 제31권2호
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• pp.61-67
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• 2021

Fabrication of a ferromagnetic composite powder for the magnesium and BaFe12O19 system by mechanical alloying (MA) is investigated at room temperature. Mixtures of Mg and BaFe12O19 powders with a weight ratio of Mg:BaFe12O19 = 4:1, 3:2, 2:3 and 1:4 are used. Optimal MA conditions to obtain a ferromagnetic composite with fine microstructure are investigated by X-ray diffraction, differential scanning calorimetry (DSC) and vibrating sample magnetometer (VSM) measurement. It is found that Mg-BaFe12O19 composite powders in which BaFe12O19 is dispersed in Mg matrix are successfully produced by MA of BaFe12O19 with Mg for 80 min. for all compositions. Magnetization of Mg-BaFe12O19 composite powders gradually increases with increasing the amounts of BaFe12O19, whereas coercive force of MA powders gradually decreases due to the refinement of BaFe12O19 powders with MA time for all compositions. However, it can be seen that the coercivity of Mg-BaFe12O19 MA composite powders with a weight ratio of Mg:BaFe12O19=4:1 and 3:2 for MA 80 min. are still high, with values of 1260 Oe and 1320 Oe compared to that of Mg:BaFe12O19=1:4. This clearly suggests that the refinement of BaFe12O19 powders during MA process for Mg:BaFe12O19=4:1 and 3:2 tends to be suppressed due to ductile Mg powders.

• Progress in Superconductivity
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• 제5권2호
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• pp.109-113
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• 2004

MgB$_2$ and FeTi composites was prepared to study the effect of FeTi particles on superconductivity of MgB$_2$. The sample, which had contained magnesium, boron and FeTi particles, was synthesized by the Commercial Stainless Steel Tube Enveloping Technique(COSSET) at 92$0^{\circ}C$ for 2 hours. The structure and properties of the sample was investigated by XRD, SEM, and SQUID magnetometer. It was found that there was a little change of T$_{c}$ compared with pure MgB$_2$ superconductor in spite of high percentage of FeTi particles, and there was no proof of structure change of MgB$_2$ superconductor due to FeTi particles. But the high porosity which was appeared in the pure MgB$_2$ was disappeared in the composites. We conclude that FeTi particles do not influence the superconductivity of MgB$_2$ and it is expected that fe-Ti material system will be a good material for a tube of the PIT process and for a substrate of the film.m.

• 한국균학회지
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• 제21권3호
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• pp.165-171
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• 1993

표고버섯 중의 광감응성 mitochondrial ATP synthase는 0.1 mM $Fe^{2+}$ 단독 이온에 의하여 그 활성이 대조구에 비해 102%, 증가되었으며, 반면 $Fe^{3+}$ 및 $Mg^{2+}$ 이온은 효소의 활성을 억제시켰다. 0.5 mM $Mg^{2+}$ 존재하에서 0.1 mM $Fe^{2+}$ 이온에 의한 이 효소의 활성은 32% 증가되었으며 0.5 mM $Mg^{2+}$ 존재하에서 $Fe^{3+}$ 이온효과는 단독 $Fe^{3+}$ 이온의 효과와 유사한 경향으로 효소의 활성을 저해하였다. 0.5 mM $Mg^{2+}$과 0.1 mM, 0.5 mM 및 1.0 mM $Fe^{3+}$ 이온의 공존하에서$Fe^{2+}$ 이온에 의한 효소의 활성은 모두 억제되었으며, 특히 0.5 mM $Mg^{2+}$과 0.1 mM $Fe^{3+}$ 이온의 공존하에서 5.0 mM $Fe^{2+}$ 이온에 의하여 53%의 억제현상을 나타내었다. 따라서 표고버섯 중의 광감응성 mitochondrial ATP synthase의 활성은 $Fe^{2+}$ 이온에 의하여 특이적으로 크게 증가되며, 이 효소에 대한 $Fe^{2+}$ 이온의 활성화 효과가 $Mg^{2+}$ 이온에 의하여 크게 영항을 받지 않으나, $Fe^{3+}$ 이온의 공존하에서는 억제됨을 알았다. 활성화 금속이온인 $Fe^{2+}$ 존재하에서 이 효소의 최적 pH는 7.6이며, 최적 온도는 $63^{\circ}C$이었다. 또한 이 효소는 금속 chelating agent인 EDTA에 의하여 효소의 활성이 상실됨으로써 metalloenzyme의 가능성을 제시하였다.

• 분석과학
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• 제14권2호
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• pp.173-179
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• 2001

K 수계 6개 지점의 퇴적물에 대해 Fe, Cu, Cr, Zn, Cd를 측정분석하였으며 분석방법들을 비교 분석하였다. 마이크로웨이브에 의한 전처리 방법이 미국의 TCLT(toxicity characteristic leaching procedure)나 폐기물공정시험방법보다 Fe, Cu, Cr, Zn, Cd 모두 높은 값을 나타내었다. 마이크로웨이브, TCLP, 폐기물 공정시험방법에 의한 중금속 분석결과 각각 38.1-48.0 mgFe/kg, 10.2-15.9 mgFe/kg, 3.5-12.6 mgFe/kg, 37.0-50.1 mgCu/kg, 0.06-0.24 mgCu/kg, 0.01-0.03 mgCu/kg 및 137.2-152.0 mgZn/kg, 0.67-0.82 mgZn/kg, 0.3-0.5 mgZn/kg으로 나타났다. 이상의 결과로부터 퇴적물 중에 오염도를 정확히 평가하기 위해서는 효율적이고 새로운 시험방법 개발 연구에 관심을 두어야 한다.

• 한국표면공학회지
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• 제37권2호
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• pp.99-109
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• 2004

The effect of trace metallic additives on microstructure, glossiness and hardness of Zinc electrodeposits was investigated by using sulfate bath and flow cell system. The preferred orientation of Zn deposits with Mg-Fe additives was (10$\ell$)+(002) mixed texture, while that of Zn deposits with Mg-Fe-Cr additives was ( $10\ell$). The preferred orientation of Zn deposits with Mg-Fe-X(X:Ni,Co) additives changed from ($10\ell$)+(002) to ($10\ell$) with increasing Mg additive from 5 to 10 g/$\ell$. The surface morphology of the Zinc deposits was closely related to the preferred orientation of the deposits. The glossiness of Zn deposits with Mg-Fe additives was similar to that of pure Zn deposit. The glossiness of Zn deposits with Mg-Fe-X(X:Ni,Cr) additives was lower than that of Zn deposits with Mg-Fe additives, while that of Zn deposits with Mg-Fe-Co additives was higher than that of Zn-Mg-Fe deposits. The hardness of Zn deposits with Mg-Fe-X(Ni,Co,Cr) increased with current density and amount of Mg additive. Hardness of Zn deposits was decreased and increased in comparison with Zn-Mg-Fe deposits for Mg-Fe-Co and Mg-Fe-Cr additives, respectively.

• 한국주조공학회지
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• 제33권2호
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• pp.55-62
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• 2013

Effect of Fe and Mn contents on the castability of Al-4wt%Mg-0.9wt%Si system alloy has been studied. According to the analysis of cooling curve for Al-4wt%Mg-0.9wt%Si-0.3wt%Fe-0.3/0.5wt%Mn alloy, ${\alpha}-Al_{15}(Fe,Mn)_3Si_2$ and ${\beta}-Al_5FeSi$ phases crystallized above eutectic temperature of $Mg_2Si$. Therefore, these phases affected both the fluidity and shrinkage behaviors of the alloy during solidification. As Fe and Mn contents of Al-4wt%Mg-0.9wt%Si system alloy increased from 0.1 wt% to 0.4 wt% and from 0.3 wt% to 0.5 wt% respectively, the fluidity of the alloy decreased by 26% and 33%. When Fe content of the alloy increased from 0.1 wt% to 0.4 wt%, 23% decrease of macro shrinkage and 19% increase of micro shrinkage appeared. Similarly, Mn content of the alloy increased from 0.3 wt% to 0.5 wt%, 11% decrease of macro shrinkage and 14% increase of micro shrinkage appeared. Judging from the castability of the alloy, Al-4wt%Mg-0.9wt%Si alloy with low content of Fe and Mn, 0.1 wt% Fe and 0.3 wt% Mn, is recommendable.