• 한국토양비료학회지
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• 제26권4호
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• pp.294-298
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• 1993

담수조건(湛水條件) 하(下)에서 환원(還元)된 토양용액(土壤溶液) 중 pH와 $Fe^{+{+}}$ 이온의 활동도(活動度) 간의 관계(關係)를 밝히기 위하여 화학적(化學的)으로 합성(合成)된 탄산철(炭酸鐵)($FeCO_3$)을 사용하여 이 관계(關係)를 실측(實測)하고 그 결과(結果)를 탄산철(炭酸鐵)의 용해도적(熔解度積), 탄산가스의 용해도상수(熔解度常數) 및 탄산($H_2CO_3$)의 해리상수(解離常數) 등을 써서 해석(解析)하고, 임의(任意)로 선정(選定)된 답토양(畓土壤) 15점을 담수항온(湛水恒溫) 시킨 후 토양용액(土壤溶液) 중 pH와 $Fe^{+{+}}$의 활동도(活動度) 간의 관계(關係)를 조사(調査)했다. 이 연구(硏究)의 주요(主要) 결론(結論)은 다음과 같다. 1. $FeCO_3-H_2O-CO_2$ 계의 pH는 탄산가스 분압(分壓)에 따라 변하며 pH와 $Fe^{+{+}}$의 활동도(活動度) 간에는 $pFe^{+{+}}=1/2pH+0.3+1/2(log\;{\gamma}HCO{_3}^--log\;{\gamma}Fe^{+{+}})$의 관계(關係)가 있다. 2. 활성철(活性鐵) 함량(含量)이 0.4 내지 1.60%이고 담수(湛水) 환원(還元)되었을 때 pH가 6.0인서 7.0 사이에 드는 우리나라에 흔히 분포(分布)하는 보통 논토양에서는 환원(還元)된 토양용액(土壤溶液) 중 $Fe^{+{+}}$의 활동도(活動度)는 탄산철의 용해도(溶解度)에 의해 결정(決定)되는 것 같다.

• 한국지하수토양환경학회지:지하수토양환경
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• 제27권1호
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• pp.25-30
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• 2022

Mackinawite (FeS), as a ubiquitous reduced iron mineral, is known as a key controller of redox reactions in anaerobic subsurface environment. The reaction of FeS with redox-sensitive toxic element such as arsenic is substantially affected by pH conditions of the given environments. In this study, the interaction of As(V) with FeS was studied under strict anaerobic conditions with various pH conditions. The pH-dependent arsenic removal tests were conducted under wide ranges of pH conditions and X-ray absorption spectroscopy (XAS) was applied to investigate the reaction mechanisms under pH 5, 7, and 9. The removal efficiency of FeS for As(V) showed the higher removal of As(V) under low pH conditions and its removal efficiency decreased with increasing pH, and no As(V) reduction was observed in 1 g/L FeS solution. However, XAS analysis indicated the reduction of As(V) to As(III) occurred during reaction between FeS and As(V). The reduced form of As(III) was particularly identified as an arsenic sulfide mineral (As₂S₃) in all pH conditions (pH 5, 7, and 9). As₂S₃ precipitation was more pronounced in pH 5 where the solubility of FeS is higher than in other pH conditions. The linear combination fitting results of XAS demonstrated that As(V) removal mechanism is concerted processes of As₂S₃ precipitation and surface complexation of both arsenic species.

• 공업화학
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• 제7권1호
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• pp.177-185
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• 1996

Fe-EDTA 착물을 이용한 황화수소 제거의 최적 반응 조건을 기포탑 반응기에서 조사하였다. 착물의 농도가 증가할수록 황화수소 산화 반응에서 전환량은 증가하였고 pH 변화와 Fe 농도는 완만하게 감소하였으며, elemental sulfur의 생성량은 증가하였다. 또한 황화수소는 0.05M 이상의 착물 농도에서 효율적으로 제거되었다. pH에 따른 황화수소 산화반응에서 pH는 착물의 안정도에 중요한 인자이고 반응 중 최적 pH 범위는 8.5~9.5 이었다. [EDTA]/[Fe] 비가 증가할수록 황화수소 산화 반응의 전환량은 증가하였고 반응 중 EDTA 농도가 감소하면 FeS로 침전이 촉진되어 전환량은 감소하였다. 즉 EDTA 농도가 증가될수록 Fe-EDTA 착물이 안정되어 전환량이 증가하였다.

• 한국분말재료학회지
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• 제25권4호
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• pp.302-308
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• 2018

A lean alloy is defined as a low alloy steel that minimizes the content of the alloying elements, while maintaining the characteristics of the sintered alloy. The purpose of this study is to determine the change in microstructure and mechanical properties due to the addition of silicon or tin in Fe-Mo-P, Fe-Mn-P, and Fe-Mo-Mn-P alloys. Silicon- or tin-added F-Mo-P, Fe-Mn-P, and Fe-Mo-Mn-P master alloys were compacted at 700 MPa and subsequently sintered under a $H_2-N_2$ atmosphere at $1120^{\circ}C$. The sintered density of three alloy systems decreases under the same compacting pressure due to dimensional expansion with increasing Si content. As the diffusion rate in the Fe-P-Mo system is higher than that in the Fe-P-Mn system, the decrease in the sintered density is the largest in the Fe-P-Mn system. The sintered density of Sn added alloys does not change with the increasing Sn content due to the effect of non-dimensional changes. However, the effect of Si addition on the transverse rupture strengthening enhancement is stronger than that of Sn addition in these lean alloys.

• 한국분말재료학회지
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• 제10권2호
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• pp.129-135
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• 2003

Nanocrystalline powders of $MnFeP_{1-x}As_x$(x=0.45-0.6) have been synthesized by mechanochemical reaction at room temperature using high-energy ball milling from mixtures of Mn, Fe, P, and As Powders. It has been found that a mechanically induced self-propagating reaction (MSR) occurs within 2 hours of milling and it produces very fine polycrystalline powder having a hexagonal $Fe_2P$ structure. Further milling up to 24 hours did not change the crystalline and average particle sizes or the phase composition of the milling product. When x is 0.65, no reaction among the reactants has been observed even after 24 hours of milling. As the P content decreases in $MnFeP_{1-x}As_x$, the incubation time for the MSR has increased and the lattice constants in both a and c axes have changed.

• 한국세라믹학회지
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• 제28권12호
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• pp.996-1004
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• 1991

In this study, we tried to synthesis iron hydroxide suitable for longitudinal magnetic recording media from waste acid, which is a by-product of an iron works factory. Effects of initial pH of reactants, reaction temperature, reaction time for the synthesis of acicular iron hydroxide were studied in relation to particle properties of iron hydroxide and magnetic properties of maghemite powders. As the pH in reactant solution increased, $\beta$-FeOOH(pH=4.5), mixture of $\beta$-FeOOH and $\alpha$-FeOOH(4.5$\alpha$-FeOOH and Fe3O4(6.4$\alpha$-FeOOH (pH>13) was found to from in order. Especially, $\alpha$-FeOOH formed above pH 13 was single phase with superior acicularity. The temperature range over which the single-phase goethite can be formed increased as the initial pH of reactants increased (pH 13:10~5$0^{\circ}C$, pH 13.2:10~7$0^{\circ}C$, pH 13.5:0~8$0^{\circ}C$). The goethite formed between 40~6$0^{\circ}C$ has superior characteristics because the acicularity increased with increasing temperature but at high temperature (>6$0^{\circ}C$) Fe3O4 (pH=13) was found to start to form. Generally, single phase of goethite was found to form after one hour when an optimized condition. The particle size of goethite did not change as the reaction time increased over one hour. Accordingly, the magnetic properties of ${\gamma}$-Fe2O3 produced from goethite were not altered.

• 대한화학회지
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• 제31권5호
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• pp.471-475
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• 1987

수용액에서 Fe(II)-poly(D-glutamic acid) (PGA) 복합물 형성이 pH와 농도에 따라서 흡수와 원이색성 분광 광도계로 확인되었으며, 철 이온과 복합물 형성에 의한 PGA의 구조 변화와 안정도 상수도 검토되었다. PGA와 Fe(II)사이에 형성된 후 pH4.3에서는 ${\alpha}$-helix를 파괴(${\alpha}$-helix 파괴 효과)하고 pH5.7에서는 ${\alpha}$-helix를 유도(${\alpha}$-helix유도 효과)하는 것을 알 수 있었다. ${\alpha}$-helix의 PGA구조가 random coil의 PGA구조 보다 전 안정도 상수 값이 큰 것으로 보아 random coil의 PGA구조에서 더욱 안정된 복합물을 형성하고 있음을 알 수 있었다.

• Elastomers and Composites
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• 제44권4호
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• pp.408-415
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• 2009

졸-겔 방법을 사용하여 Fe-ACF/$TiO_2$ 복합체 광촉매를 제조하였다. 여러 가지 철 전구체를 사용하여 세가지 Fe-ACF/$TiO_2$ 복합체를 제조하고 BET, SEM, XRD 및 EDX를 사용하여 특성화 하였다. UV 조사에서 Rh.B 용액의 분해에 의거하여 Fe-ACF/$TiO_2$ 복합체의 광촉매 특성을 파악 하였다. 실험 결과로부터, Fe-ACF/$TiO_2$ 복합체는 ACF/$TiO_2$ 복합체 보다 Rh.B의 제거 효과가 더 우수함을 나타내었다. 또한 여러 가지 Fe 전구체 사용으로 인한 Fe 원소의 포토-펜톤 효과는 다르게 나타났다. $FeCl_3$을 사용하여 제조된 Fe-ACF/$TiO_2$ 복합체는 가장 우수한 포토-펜톤 효과를 나타내었고, pH 변화에 의존하여 Rh.B 용액 분해에 대하여 영향을 주었다.

• 한국물환경학회지
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• 제22권2호
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• pp.328-332
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• 2006

Fe(III)-impregnated activated carbon (Fe-AC) was applied in the treatment of synthetic wastewater containing Cu(II). To investigate the stability of Fe-AC at acidic condition, dissolution of Fe was studied with a variation of solution pH ranging from 2 to 4. Fe-AC was unstable at pH 2, showing a gradual increase of the dissoluted Fe as reaction time increased, while negligible amount of Fe was dissoluted above pH 3. This stability test suggests the applicability of Fe-AC in the treatment of wastewater above pH 3. Adsorption capacity of Cu(II) onto activated carbon (AC) and Fe-AC was investigated in a batch and a column test. In the adsorption kinetics, rapid adsorption of Cu(II) onto AC and Fe-AC was noted at initial reaction time and then reached a near complete equilibrium after 6 hrs. Adsorption trends of Cu(II) onto AC and Fe-AC were similar, showing an increased Cu(II) adsorption at higher pH. Compared with AC, Fe-AC showed a greater Cu(II) adsorption over the entire pH range studied in this research. From the adsorption isotherm obtained with variation of the concentration of Cu(II), the maximum adsorption capacity was identified as 61,700 mg/kg.

• 대한전기학회논문지:전기물성ㆍ응용부문C
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• 제50권1호
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• pp.1-5
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• 2001

P(VDF/TrFE) copolymer thin films with 70/30 and 80/20 mol% VDF (polyvinylidene fluoride) and TrFE (trifluoroethylene) rates were prepared by using a vapor deposition method, During thin films were prepared, the substrate temperatures were maintained at 30 $^{\circ}C$ and 120 $^{\circ}C$, and the heating source temperature was fixed at 350 $^{\circ}C$. Contary to PVDF homopolymer, P(VDF/TrFE) copolymers showed the Curie point(Tc) below the melting point. The Curie point (Tc) and the melting point of the P(VDF/TrFE) copolymers were changed as a function of substrate temperature and the VDF mol%. The Curie point and the melting point of P(VDF/TreFE) thin films decreased and increased with increasing substrate temperature, respectively. Also with increasing VDF mol%, the melting point decreased slightly, however the Curie point increased.