• 한국환경과학회지
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• 제28권1호
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• pp.99-106
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• 2019

Arsenic is among the heavy metals commonly found in aqueous environments. Iron oxide is known as an efficient adsorbent for the arsenic. A new synthetic method was applied to provide iron oxide giving a large specific surface area. The mixing method affects the formation of iron oxide. Ultrasonic waves assisted the formation of very fine iron oxide in an organic phase. The synthesized iron oxide is amorphous type with a high surface area of more than $181.3m^2/g$. Sorption capacity of the synthesized adsorbent was relatively very high for arsenic and varied depending on the oxidation state of arsenic: a higher capacity was obtained with As(V). Lower solution pH provided a higher sorption capacity for As(V). The competitive effect of co-exist anions such as chloride, nitrate, and sulfate was minimal in sorption capacity of the iron oxide for arsenic.

• 한국세라믹학회지
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• 제27권1호
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• pp.109-117
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• 1990

Magnetite for Water-based ferrofluid was synthesized by air oxidation of aqueous suspension in the pH range 7-12 at $65^{\circ}C$. The optimum condition of magneite formation was delineated by examining various physicochemcial properties such as Fe2+ content, phase characteristics, MHC and $\sigma$max. The point of zero charge of iron oxide powders obtained at various pH conditions were correlated with the oxidation state of Fe in the iron oxide. The magnetite powder prepared at pH 9 ws dispersed using sodium oleate and sodium dodecylbenzenesulfonate (SDBS) as dispersants, and the dispersion characteristics of the magnetite ferrofluid were examined by means of the fraction of solid dispersed, zeta potential data and FT-IR spectrum. A simple calculation on the potential energy of two interacting magnetite particles showed that the dispersion stability was directly correlated with height of the potential energy barrier or the shape of zeta potential.

• 한국세라믹학회지
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• 제52권2호
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• pp.133-136
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• 2015

The outward diffusion of $Na^+$ ions in iron-bearing soda lime silicate glass via oxidation heat treatment before the ion exchange process is artificially induced in order to increase the amount of ions exchanged during the ion exchange process. The effect of the addition process is analyzed through measuring the bending strength, the weight change, and the inter-diffusion coefficient after the ion exchange process. The glass strength is increased when the outward diffusion of $Na^+$ ions via oxidation heat treatment before the ion exchange process is added. For the glass subjected to the additional process, the weight change and diffusion depth increase compared with the glass not subjected to the process. The interdiffusion coefficient is also slightly increased as a result of the additional process.

• Bulletin of the Korean Chemical Society
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• 제16권5호
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• pp.398-400
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• 1995

Selective oxidation of cyclohexane in acetone solution has been studied using iron catalysts with hydrogen peroxide in-situ produced by palladium catalyst. Iron tetraphenylporphyrin chloride shows the highest activity among the tested chlorides and porphyrin complexes of some metals of the first transiton series. Iron chloride and iron tetraphenylporphyrin chloride were supported on four kinds of 4-vinylpyridine copolymer with styrene or divinyl-benzene. Nitrogen 1s photoelectron spectra give the evidence that pyridyl nitrogens of the 4-vinyl pyridine copolymer act as ligands to bind iron species. The copolymer with styrene is the most efficient support for the binding because its solubility in catalyst preparation solvent (methylene chloride) gives the pyridyl group advantage to contact with the iron catalysts. However, better catalytic activity per iron atom could be obtained with a rigid crosslinked polymer due to active site isolation.

• KSBB Journal
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• 제16권1호
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• pp.54-60
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• 2001

저품위 광석으로부터 유가 금속을 회수하기 위한 생물용출법의 적용에 있어 미생물의 활성은 매우 중요하며, 제련미생물은 금속이온에 대해 어느 정도 내성을 가지고 있어야 한다. 본 연구에서는 대표적인 제련미생물인 Thiobacillus ferrooxidans의 철산화속도에 미치는 단독 혹은 혼합 금속이온의 영향을 조사하여, T. ferrooxidans의 금속이온에 대한 내성 특성을 조사하였다. 생장 배지에 $Zn^{2+}$, $Cu^{2+}$, $Ni^{2+}$, 및 $Cd^{2+}$를 단독으로 첨가한 경우(첨가농도범위, $Zn^{2+}$ 60g/L이하, $Cu^{2+}$, $Ni^{2+}$, 및 $Cd^{2+}$ 6 g/L 이하)에는 T. ferrooxidans에 의한 철산화속도는 금속이온의 첨가량에 크게 저해 받지 않았다. $Zn^{2+}$를 제외한 $Cu^{2+}$, $Ni^{2+}$, 및 $Cd^{2+}$의 2 성분 혹은 3 성분의 혼합금속이온을 첨가한 경우에는 T. ferrooxidans의 철산화 활성에 대한 혼합 금속이온의 저해 효과는 최대 50% 정도로 크게 나타나지는 않았다. 그러나, $Zn^{2+}$을 타 금속이온과 2 성분 혹은 3 성분을 혼합하여 생장 배지에 첨가한 경우에는 T. ferrooxidans의 철산화 활성 저해에 대한 혼합 금속이온의 상승 효과가 큰 것을 밝혔다.

• 충청수학회지
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• 제27권2호
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• pp.319-325
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• 2014

In this paper, we investigate chemical hyperstructures of chemical reactions for iron and indium using hyperstructure theory.

• 한국환경농학회:학술대회논문집
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• 한국환경농학회 2009년도 정기총회 및 국제심포지엄
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• pp.350-351
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• 2009

• 한국지하수토양환경학회지:지하수토양환경
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• 제22권1호
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• pp.41-48
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• 2017

Persulfate (PS) activated with nanosized zero-valent iron (NZVI) was tested as a reagent to remove phenol from groundwater. Batch degradation experiments indicated that NZVI/PS molar ratios between 1 : 2 and 1 : 5 were appropriate for complete removal of phenol, and that the time required for complete removal varied with different PS and NZVI dosages. Chloride ions up to 100 mM enhanced the phenol oxidation rate, and nitrate of any concentration up to 100 mM did not significantly affect the oxidation rate. NZVI showed greater performance than ferrous iron did as an activator for PS. A by-product was formed along with phenol degradation but subsequently was completely degraded, which showed the potential to attain mineralization with the NZVI/PS system. Tests with radical quenchers indicated that sulfate radicals were a predominant radical. The results of this study suggest that NZVI is a promising activator of PS for treating contaminated groundwater.

• 대한금속재료학회지
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• 제47권2호
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• pp.107-113
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• 2009

Molten iron with 2 mass % carbon content was decarbonized at 1823 K~1923 K by bubbling $Ar+O_2$ gas through a submerged nozzle. The reaction rate was significantly influenced by the oxygen partial pressure and the gas flow rate. Little evolution of CO gas was observed in the initial 5 seconds of the oxidation; however, this was followed by a period of high evolution rate of CO gas. The partial pressure of CO gas decreased with further progress of the decarbonization. The overall reaction is decomposed to two elementary reactions: the decarbonization and the dissolution rate of oxygen. The assumptions were made that these reactions are at equilibrium and that the reaction rates are controlled by mass transfer rates within and around the gas bubble. The time variations of carbon and oxygen contents in the melt and the CO partial pressure in the off-gas under various bubbling conditions were well explained by the mathematical model. Based on the present model, it was explained that the decarbonization rate of molten iron was controlled by gas-phase mass transfer at the first stage of reaction, but the rate controlling step was transferred to liquid-phase mass transfer from one third of reaction time.

• 자원환경지질
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• 제34권1호
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• pp.147-156
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• 2001

티탄자철석(titanomagnetite)은 해양지각을 이루는 현무암에 존재하는 중요한 자성광물로서 일반적으로 저온산화에 의해 양이온이 결핍된(cation-deficient) 티탄맥히마이트(titanomaghemite)로 변한다. 실험실에서 철성분 제거방식(removal of iron mechanism)을 통해 자연에서 일어나는 티탄자철석의 수성 저온산화(low-temperature aqueous oxidation)를 재현하였으며, 산화정도에 따라 티탄맥히마이트의 자기적 특성이 민감하게 변화하는 것을 관찰하였다. 본 실험 결과 산화정도에 따라 티탄자철석의 큐리온도(Tc)는 166$^{\circ}C$에서 40$0^{\circ}C$로 증가하였고, 상온에서의 포화자화 강도(Ms)는 126.30 kA/m(25.26 emu/g)에서 16.55 kA/m(3.31 emu/g)로 감소하였으며, 항자기력(Hc)은 6.13 kA/m(77 Oe)에서 38.83 kA/m (488 Oe)로 잔류항자기력(Hcr)은 23.24 kA/m(292 Oe)에서 47.03 kA/m(591 Oe)로 증가함을 관찰하였다. 또한 대자율($\chi$)은 $2023{\times}10^{-6}SI$에서 $84{\times}10^{-6}SI$로 감소함을 나타내었다. 이와 같은 결과를 근거로 현재에서 30 Ma까지의 해양지각의 자화 강도의 변화는 티탄자철석의 저온산화에 의한 결과로 해석하였으며 30~120 Ma에 이르는 해양지각의 자화 강도의 변화는 해양지각에 포함된 티탄자철석의 산화와 산화에 순반되는 광물전에 의한 결과로 추정하였으며 보다 구체적인 원인은 해양지각에서 채취한 시료에 대한 체계적인 연구를 통해서 밝혀질 것으로 기대된다.