• 한국세라믹학회지
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• 제17권2호
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• pp.89-95
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• 1980

The effect of non-stoichimetry and sintering temperature on the magnetic properties of materials in the system $Ni_{0.39}Zn_{0.61}Fe_{2.0+x}O_4$ have been investigated. The value of x used in initial weighing of oxides were varied from -0.04 to -0.12. The value of x, however, appears to be from +0.04 to -0.04 after ferrite powder preparation due to iron pick up during ball mill mixing and grinding. The densities of specimens which were deficientinrion were higher than those with excess ion. Specimens with near stoichiometric composition showed maximum initial permeability an dminimum coercivity whereas high values of quality factor (Q) were observed in iron deficient specimens. The quality factor decreased monotonically with increasing sintering temperature, but the permeability showed maxima with increasing sintering temperature. Thus highest value of figure of merit $\mu$Q was obtained in composition $Ni_{0.39}Zn_{0.61}Fe_{1.98O4}$ sintered at 100$0^{\circ}C$ for 3 hrs. in an air atmosphere.

• 한국식품과학회지
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• 제33권5호
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• pp.626-632
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• 2001

식물체(팽이버섯, 마늘, 녹차, allspice, 하수오, 오미자, 행인, 솔잎)가 free radical 반응 및 지방산화 억제에 미치는 영향과 nitrosamine 생성의 직접적인 영향인자인 아질산염에 대한 천연물의 분해효과를 검토한 결과 각 추출물의 pH는 열수추출물보다 ethanol추출물이 높은 pH를 나타내었으며, 그중에서 오미자 열수추출물이 3.0으로 가장 낮았다. 지방산화의 촉진인자인 $Fe^{2+}$ 이온과 활성산소 중 지방산화를 일으키는데 주요한 역할을 하는 hydroxyl radical에 대한 각 추출물들의 영향은 추출물 모두 $Fe^{2+}$ 이온 binding 능력은 탁월하였으며, deoxyribose상에서 OH 포집능 측정에서도 팽이버섯, 솔잎ethanol추출물이 다른 추출물에 비하여 낮은 TBARS값을 나타내었다. Iron의 함량은 열수추출물에서는 2.0 mg/100 g 미만이었으나, 오미자 추출물의 total iron 함량이 6.8 mg/100 g으로 가장 높게 나타났다. 용매별 iron함량 측정에서는 ethanol 추출물의 iron함량이 전반적으로 열수추출물보다 낮은 iron함량을 나타내었다. Ascorbic acid 함량은 녹차추출물이 열수 및 ethanol 추출에서 각각 14.3 mg/100 g, 16.7 mg/100 g을 나타내어 가장 높은 함량을 나타내었다. 전자공여능은 팽이버섯, 마늘 추출물을 제외하고 50% 이상의 전자공여능을 나타내었으며, 열수추출보다는 ethanol 추출물의 전자공여능이 우수하였다. SOD 유사활성은 전반적으로 8%이상의 활성능을 보였으나, 솔잎 ethanol추출물은 활성능이 미미하였으며. 녹차 열수와 ethanol추출물이 각각 85.3%, 63.5%로 가장 높은 활성능을 나타내었다. 아질산염 소거작용은 열수추출물이 전반적으로 ethanol추출물에 비하여 높은 소거능을 나타내었다. 녹차추출물의 열수와 ethanol 추출물은 아질산염 소거능이 매우 우수하였다.

• 환경위생공학
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• 제22권3호
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• pp.77-87
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• 2007

The ion exchange resins have been synthesized from chlormethyl styrene - 1,4 - divinylbenzene(DVB) with 1%, 3%, and 5%-crosslinking and macro cyclic ligand of OenNen-$H_4$ by copolymerization method and the adsorption characteristics of uranium(VI), iron(II) and samarium(III) metallic ions have been investigated in various experimental conditions. The synthesis of these resins was confirmed by content of chlorine, element analysis, and IR-spectrum. The effects of pH, time, dielectric constant of solvent and crosslink on adsorption of metallic ions were investigated. The uranium ion was showed fast adsorption on the resins above pH 3. The optimum equilibrium time for adsorption of metallic ions was about two hours. The adsorption selectivity determined in ethanol was in increasing order uranium ${UO_2}^{2+}>Fe^{2+}>Sm^{3+}$ ion. The adsorption was in order of 1%, 3%, and 5% crosslink resin and adsorption of resin decreased in proportion to order of dielectric constant of solvent.

• 한국자동차공학회논문집
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• 제22권1호
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• pp.135-141
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• 2014

$NH_3$-SCR has high NOx removal efficiency approximately 80~90%. Recently, the copper or iron ion-exchanged zeolite catalysts are widely used as automobile SCR catalysts. In this paper, the effect of the space velocity, temperature of reaction and $NO_2$ addition on the $NH_3$-SCR reaction were studied using various zeolite SCR catalysts. The test was conducted with small sized fresh catalysts in a laboratory fixed-bed flow reactor system using simulated gases. It is found that the activity of the BEA is better than MFI. It seems that three-dimensional framework and a wide pore entrance of BEA enhances the SCR activity. It is also found that low temperature activity of Cu-zeolites was better than Fe-zeolites. Once $NO_2$ was added, the NOx conversion activity of the Cu-zeolite was slightly enhanced, whereas remarkable improvement was achieved by Fe-zeolite.

• 펄프종이기술
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• 제40권5호
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• pp.42-46
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• 2008

The papers in preserved books and archives experience aging which was affected by a variety of factors. Thus, the studies concerning impacts of those factors on paper aging are required. In this research, a simulation of a short-time accelerated paper aging was conducted in order to examine the effects of acid and metals (alum, copper (II) sulfate, copper (II) chloride, and iron (III) chloride) on the natural paper aging for a long time. As a result of experiments, it is found that both acid and metals have impacts on paper aging. Alum resulted in the significant decrease of pH, brightness, folding endurance, and viscosity of paper. Both copper (II) chloride and iron (III) chloride also resulted in the decrease of brightness, folding endurance, and viscosity of paper. In more detail, paper aging by iron (III) chloride showed much more significant than that by copper (II) chloride. The paper aging in case of copper (II) sulfate coexisting sulfate ion, where metal absorbed moisture was higher than in case of paper treated only by alum. This result indicated that metal catalyzes paper aging by acid. Based on these results, it was revealed that both alum and metal are the major factors in paper aging. In particular, paper aging was far more accelerated in case when acid and metals existed in paper at the same time.

• 한국지하수토양환경학회지:지하수토양환경
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• 제25권1호
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• pp.62-73
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• 2020

PAHs commonly found in industrial sites such as manufactured gas plants (MGP) are potentially toxic, mutagenic and carcinogenic, and thus require immediate remediation. In-situ chemical oxidation (ISCO) is known as a highly efficient technology for soil and groundwater remediation. Among the several types of oxidants utilized in ISCO, persulfate has gained significant attention in recent years. Peroxydisulfate ion (S₂O₈^2-) is a strong oxidant with very high redox potential (E⁰ = 2.01 V). When mixed with Fe²⁺, it is capable of forming the sulfate radical (SO₄^-·) that has an even higher redox potential (E⁰ = 2.6 V). In this study, the influence of various iron activators on the persulfate oxidation of PAHs in contaminated soils was investigated. Several iron sources such as ferrous sulfate (FeSO₄), ferrous sulfide (FeS) and zero-valent iron (Fe(0)) were tested as a persulfate activator. Acenaphthene (ANE), dibenzofuran (DBF) and fluorene (FLE) were selected as model compounds because they were the dominant PAHs found in the field-contaminated soil collected from a MGP site. Oxidation kinetics of these PAHs in an artificially contaminated soil and the PAH-contaminated field soil were investigated. For all soils, Fe(0) was the most effective iron activator. The maximum PAHs removal rate in Fe(0)-mediated reactions was 92.7% for ANE, 83.0% for FLE, and 59.3% for DBF in the artificially contaminated soil, while the removal rate of total PAHs was 72.7% in the field-contaminated soil. To promote the iron activator effect, the effects of hydroxylamine as a reducing agent on reduction of Fe³⁺ to Fe²⁺, and EDTA and pyrophosphate as chelating agents on iron stabilization in persulfate oxidation were also investigated. As hydroxylamine and chelating agents (EDTA, pyrophosphate) dosage increased, the individual PAH removal rate in the artificially contaminated soil and the total PAHs removal rate in the field-contaminated soil increased.

• 보존과학회지
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• 제33권5호
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• pp.381-390
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• 2017

철제유물의 안정화처리는 탈염을 중점으로 하고 있으나, 부식인자 제거여부의 불확실성과 일부 유물의 제한적 적용 등으로 재부식과 같은 문제점이 지적되고 있다. 이를 보완하기 위한 부식억제제의 연구는 일부 보고된 바 있으며, 이 연구는 부식억제를 위한 수처리제 3종에 대한 연구결과이다. 부식억제제 피막이 형성된 시편의 표면관찰 결과 인산염이 주성분인 1종 2호의 시편은 표면의 녹층이 제거되었고, 재부식 시편의 중량 감소율 평균은 1종 2호의 경우 0.58%, 2종 2호의 경우 0.03%, 3종 2호의 경우 0.07%이며, 부식인자인 $Cl^-$ 이온의 변화량은 1종 2호는 28.60 ppm, 2종 2호는 -4.08 ppm, 3종 2호는 -1.94 ppm이었다. 수처리제의 피막에 대하여 XPS로 표면상태를 분석한 결과, 3종 2호보다 2종 2호에서 소지금속인 Fe가 낮게 검출되어 다소 우수한 피막을 유지하였고, Si함량에서도 규산염 기반의 2종 2호에서 상대적으로 함량이 높아 피막 형성이 우수하다고 판단된다. 인산염을 주성분으로 한 1종 2호는 표면의 녹층을 제거하여 금속유물 보존처리약품으로 부적합하고, 규산염을 주성분을 한 2종 2호와 3종 2호의 수처리제는 부식억제 효과가 우수하다고 평가된다. 부식억제제는 철제유물의 출토 당시에 긴급하게 사용할 수 있는 약품으로도 활용이 가능할 것이다.

• Bulletin of the Korean Chemical Society
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• 제21권5호
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• pp.503-509
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• 2000

The solvent effects on the relative free energies of solvation and the difference in partition coefficients (log P) for $Rb^+$ to $K^+$ mutation in several solvents have been investigated using Monte Carlo simulation (MCS) of statistical perturbation theory(SPT). In comparing the relative free energies for interconversion of one ion pair, $Rb^+$ to $K^+$, in $H_2O$(TIP4P) in this study with the relative free energies of the computer simulations and the experimental, we found that the figure in this study with the relative free energies of the computert simulations and the experimental, we found that the figure in this study is $-5.00\pm0.11$ kcal/mol and those of the computer simulations are $-5.40\pm1.9$, -5.5, and -5.4 kcal/mol. The experimental is -5.1 kcal/mol. There is good agreement among various studies, taking into account both methods used to obtain the hydration free energies and standard deviations. There is also good agreement between the calculated structural properties of this study and the simulations, ab initio and the experimental results. We have explained the deviation of the relationship between the free energy difference and the Onsager dielectric function of solvents by the electron pair donor properties of the solvents. For the $Rb^+$ and $K^+$ ion pair, the Onsager dielectric function of solvents (or solvent permittivity), donor number of solvent and the differences in solvation dominate the differences in the relative free energies of solvation and partition coefficients.

• International Journal of Concrete Structures and Materials
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• 제4권2호
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• pp.71-75
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• 2010

The chloride ion attack on the passive iron oxide layer of reinforcement steel embedded in concrete under variable temperature environment is influenced by several parameters and some of them still need to be further investigated in more detail. Different school of thoughts exist between past researchers and the data is limited in the high temperature and high chloride concentration range which is necessary with regards to setting boundary conditions for enhancement of tafel diagram model presented in this research. The objective of this paper is to investigate the detrimental coupled effects of chloride and temperature on corrosion of reinforced concrete structures in the high range by incorporating classical Tafel diagram chloride induced corrosion model and laboratory controlled experimental non-linear effect of temperature on corrosion of rebar embedded in concrete.

• Corrosion Science and Technology
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• 제12권1호
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• pp.40-49
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• 2013

Effects of magnesium and pH on corrosion of aluminum galvanically coupled to iron have studied by using potentio- dynamic and static tests for polarization curves, Mott-Schottky test for analysis of semiconductor property, and GD-AES and XPS for film analysis. Pitting potential was sensitive to magnesium as an alloying element but not to pH, while passive current was sensitive to pH but not to magnesium. It was explained with, instead of point defect model (PDM), surface charge model describing that the ingression of chloride depends on the state of surface charge and passive film at film/solution interface is affected by pH. In addition, galvanic current of aluminum electrically coupled to iron was not affected by magnesium in pH 8.4, 0.2M citrate solution but was increased by magnesium at the solution of pH 9.1. The galvanic current at pH 9.1 increased with time at the initial stage and after the exposure of about 200 minute, decreased and stabilized. The behavior of the galvanic current was related with the concentration of magnesium at the surface. It agreed with the depletion of magnesium at the oxide surface by using glow discharge atomic emission spectroscopy (GD-AES). In addition, pitting potential of pure aluminum was reduced in neutral pH solution where chloride ion maybe are competitively adsorbed on pure aluminum. It was confirmed by the exponential decrease of pitting potential with log of [$Cl^-$] around 0.025 M of [$Cl^-$] and linear decrease of the pitting potential. From the above results, unlike magnesium, alloying elements with higher electron negativity, lowering isoelectric point (ISE), are recommended to be added to improve pitting corrosion resistance of aluminum and its alloys in neutral solutions as well as their galvanic corrosion resistance in weakly basic solutions.