• Resources Recycling
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• v.27 no.1
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• pp.38-44
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• 2018

A large amount of Nd-Fe-B magnet scraps are generated during magnet manufacture process. In this study, selective chlorination of the rare earth elements by hydrogen chloride gas which obtained from the pyrolysis of polyvinyl chloride (PVC) was investigated. In thermogravimetric analysis, drastic weight loss was occurred at about 500 K and 710 K. At the isothermal experiments, the weight loss reaches about 30% above 673 K. XRD patterns characterized that after each experiments, ${\alpha}$-Fe, Nd oxychloride, Nd chloride, and Fe chlorides were formed, and the leaching residues remain only ${\alpha}$-Fe. The yields of Nd, Dy, and Fe for the isothermal experiment were increased with temperature and peaked at 873 K. As PVC ratio increased, the yields of Nd, Dy and Fe were also increased.

• Journal of the Korean Electrochemical Society
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• v.15 no.4
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• pp.256-263
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• 2012

This study was performed to investigate the separation of cesium cations by using an electrochemical ion exchanger of nickel hexacyanoferrate($KNiFe(CN)_6$) film electrode. Potential, current, and charge passing through the cyclic voltammograms were measured in singular and binary solutions of 1.0M $NaNO_3$ and 1.0M $CsNO_3$. Before and after each experiment, the structural morphology and atomic composition of $KNiFe(CN)_6$ were analyzed by SEM and EDS, respectively. The ion selectivity of $KNiFe(CN)_6$ was also observed by the voltammograms and atomic compositions measured in the solution alternated between sodium and cesium. As the result of this study, it was found that the electrically switched $KNiFe(CN)_6$ ion exchanger had the significant advantage of 40 times or longer durability than conventional organic or inorganic ion exchanger. It was also shown that the $KNiFe(CN)_6$ ion exchanger had high selectivity for cesium over sodium.

• 한국전기화학회:학술대회논문집
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• 1999.04a
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• pp.61-61
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• 1999

• Journal of Applied Tourism Food and Beverage Management and Research
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• v.17 no.2
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• pp.95-106
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• 2006

Iron was bound by neutral detergent fiber(NDF) obtained from 15 kinds of vegetables being consumed commonly in Korea. Binding capacity of Fe of NDF ranged from 37.83% to 85.51%. Fe binding capacity of NDF increased as pH increased and reached to a maximum at pH 7 in all vegetables. The amount of Fe bound to NDF increased as Fe concentration increased.

• Proceedings of the Korean Environmental Sciences Society Conference
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• 2007.05a
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• pp.61-64
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• 2007

Fe-PC와 Fe-TCPC를 합성하여 암모니아 탈착에 따른 촉매의 특성과 황화합물 및 아민류의 흡착실험을 수행하여 다음과 같은 결론을 얻었다. 1) FT-IR로 분석한 결과, Fe-TCPC는 Fe-PC에 비해 카르복실기의 특성 스펙트럼이 관찰되었고, SEM/EDS로 관찰한 결과 카르복실기의 영향으로 Fe의 비율이 낮고 산소의 량은 높게 나타났으므로 표면에 카르복실기가 존재하고 있음을 알 수 있었다. 2) TPD 실험에서 철 프탈로시아닌 유도체는 두 개의 피크가 저온부와 고온부에서 나타나 약산점과 강산점이 존재하고 있음을 확인 할 수 있었으며, 탈착량은 Fe-TCPC가 Fe-PC보다 고온부에서 강산량점량이 많았고 저온부에서 약산점량은 적게 나타난 것으로 보아 Fe-TCPC가 표면에 카르복실기의 화학적흡착 영향으로 강산점에서 많은 탈착이 일어났음을 의미한다. 3) Fe-TCPC는 Fe-PC보다 비표면적과 세공부피가 많았고, 과산화수소의 분해효율이 높아 촉매적 성질이 우수하였으며, 또한 입자의 크기도 작았음을 확인하였다. 이는 모든 조건에서 Fe-TCPC가 Fe-PC보다 흡착능력이 우수한 것으로 예측된다. 4)카르복실기가 치환된 철 프탈로시아닌 유도체의 제거효율은 아민화합물이 우수하지만 황화합물에서 다소 낮게 나타났다. 이 결과로 보아 아민류에 효과가 있는 카르복실 철 프탈로시아닌을 착색제로 사용하면 탈취 기능을 가진 안료가 될 것으로 생각된다.

• Journal of Korean Society of Environmental Engineers
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• v.30 no.3
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• pp.345-351
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• 2008

Fe-impregnated activated carbon(Fe-AC) was prepared by Fe(III) loading on activated carbon(AC) in various preparation pH. In order to evaluate the stability of Fe-AC, dissolution of iron from Fe-AC in acidic conditions was measured. In addition, batch experiments were conducted to monitor the removal efficiency of copper by Fe-AC. Results of stability test for Fe-AC showed that the amount of extracted iron increased with contact time but decreased with increasing solution pH. The dissolved amount of iron gradually increased at solution pH 2 and finally 13% of the total iron loaded on activated carbon was extracted after 12 hr. However dissolution of iron was negligible over solution pH 3. Removal of Cu(II) by Fe-AC was greatly affected by solution pH and was decreased as solution pH increased as well as initial Cu(II) concentration decreased. Surface complexation modeling was performed by considering inner-sphere complexation reaction and using the diffuse layer model with MINTEQA2 program.

• Journal of Korean Society of Environmental Engineers
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• v.29 no.7
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• pp.778-782
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• 2007

This study investigated the dechlorination mechanisms of TCE by Fe(II) associated with cement. Batch slurry experiments were peformed to investigate the behaviors of selected ions; Fe(II), Fe(III), $Ca^{2+}$, $SO_4^{2-}$ in cement/Fe(II) system. The kinetic experiments of TCE in cement/Fe(II) systems showed that injected Fe(II) was mostly sorbed on cement within 0.5 day and 90% of injected 200 mM sulfate was sorbed on cement within 0.5 day when $[TCE]_0$ = 0.25 mM and $[Fe(II)]_0$ = 200 mM. The kinetic experiments of TCE in hematite/CaO/Fe((II) systems were conducted for simulation of cement/Fe(II) system. Calcium oxide that is one of the major components in cement hydration reactions or has a reactivity in limited conditions. Hematite assumed the ferric iron oxide component of cement. The reactivities observed in hematite/CaO/Fe(II) system were comparable to those reported for cement/Fe(II) systems containing similar molar amounts of Fe(II). The behavior of Fe(II) and $SO_4^{2-}$ sorbed on solid phase at an early stage of reaction in hematite/CaO/Fe(II) system was similar to that of cement/Fe(II) system. Ferric ion was released from hematite at an early period of reaction at low pH. The experimental evidence of kinetic test using hematite/CaO/Fe(II) system implies that the reactive reductant is a mixed-valent Fe(II)-Fe(III) mineral, which may be similar to green rust. Fe(II) sorbed on cement can be converted to new mineral phase having a reactivity such as Fe(II)-Fe(III) (hydr)oxides in cement/Fe(II) systems.

• Proceedings of the Computational Structural Engineering Institute Conference
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• 2011.04a
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• pp.598-601
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• 2011

동적응답과 하중을 정확히 산정하기 위해서는 구조물의 동적특성을 정확히 평가하는 것이 중요하기 때문에, 현재 대부분의 경우 FE 모델을 이용한 Modal 해석을 dldydg하여 동특성을 평가하고 있다. 그러나 실제 건물의 계측결과와 동적특성의 해석결과가 많은 차이를 나타내고 있으므로 해석결과의 신뢰성을 향상하기 위해서는 FE 모델에 대한 Calibration이 수행될 필요성이 있다. 이 논문에서는 초고층, 아파트, 대공간 구조물에 대한 계측을 수행하고 이 결과를 바탕으로 동특성을 정확히 예측하기 위한 FE 모델의Calibration 과정을 제시하였다. 이 결과를 바탕으로 동적특성의 정확성이 풍동실험결과의 신뢰성에 미치는 영향을 분석하였다.

• Corrosion Science and Technology
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• v.14 no.1
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• pp.19-24
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• 2015

Flow Accelerated Corrosion (FAC) causes unexpected accidents in a secondary side of a nuclear power plant. The secondary side pipes are mainly carbon steel tubes that have a protective magnetite ($Fe_3O_4$) layer on the inner surface. The stability of the protective magnetite layer depends on the parameters related to the FAC phenomena such as pH, temperature, flow rate, surface roughness etc. The dissolution of magnetite is basically the electrochemical reaction, but the most of the experiments of magnetite dissolution were carried out thermodynamically to determine the solubility of magnetite. The knowledge of the electrochemical properties of magnetite is required to understand the dissolution process of magnetite. This paper reviews the manufacture of the magnetite ($Fe_3O_4$) electrode, and summaries the electrochemical properties of the magnetite.

• Journal of the Korean Magnetics Society
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• v.16 no.1
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• pp.1-5
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• 2006

The crystallographic properties and cation distribution of oxyspinels ferrite $Co_xFe_{1-x}O_4$ thin films have been explored by X-ray diffraction, vibrating sample magnetometer (VSM), and conversion electron $M\"{o}ssbauer$ spectroscopy (CEMS). Thin films are prepared by sol-gel method. Normal spinel structure is transformed to inverse spinel structure with increasing Co concentration CEMS results indicate that most of $Fe^{3+}$ ions are substituted to $Co^{3+}$ions. Accordingly $Co^{2+}$ ions on octahedral site migrate to tetrahedral site. Magnetic moment is decreased with increasing Co concentration, which means high spin $Fe^{3+}$ ions are replaced by low spin $Co^{3+}$.