• 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 the Korean Ceramic Society
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• v.56 no.6
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• pp.577-582
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• 2019

Recently, E-glass fiber is the one of most widely used ceramic fiber for aerospace fields. Recycling technology for waste of wind power blades is arising issue for reasons of low manageability and high cost of wastes. Though glass fiber is perfectly dissolved in hydrofluoric acid, low cost for recycling and harmless to human is important for recycling of blades. Chemically melted glass fiber will be used as different purpose like accelerator of hardening for shotcrete. In this study, dissolution process of glass fiber is tested in NaOH solution at low temperatures. In addition, difference in diameter reduction of glass fiber is observed by various alkali concentration and reaction times, treatment temperatures using FE-SEM.

• Journal of the Mineralogical Society of Korea
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• v.32 no.4
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• pp.303-312
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• 2019

In this study, X-ray diffraction, ICP analysis, and leaching experiments were performed to analyze the heavy metals and dissolution characteristics of Andong dam sediments. As a result of X-ray diffraction analysis, Andong dam sediment consists of quartz, plagioclase, chlorite and illite. ICP analysis of sediment showed very high concentrations of As and Cd. Leaching experiments were performed in aerobic and anaerobic condition in a disturbed state. The results of leaching experiment showed that more heavy metals were leached in aerobic than anaerobic conditions. Heavy metal that increased in concentration with time in aerobic conditions were Mn, Zn and Cd, and those in anaerobic conditions were Mn, Fe and As. The leaching ratio of heavy metal concentration in sediment was Mn > Cd > Zn > Ni > Cu > As > Pb ≒ Fe ≒ Cr and Mn > As > Cu > Ni > Zn > Pb ≒ Cd ≒ Fe ≒ Cr in aerobic and anaerobic conditions, respectively.

• Corrosion Science and Technology
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• v.7 no.6
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• pp.315-318
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• 2008

The atmospheric corrosion performance of Al-alloying, Si-alloying and Al-Si-alloying steel were studied by wet/dry cyclic corrosion tests (CCT) at $30^{\circ}C$ and 60% relative humidity (RH). The corrosion electrolyte used for CCT was 0.052 wt% $NaHSO_{3}$ (pH~4) solution. The result of gravimetry demonstrated that Al-Si-bearing steels showed lower corrosion resistance than other rusted steels. But the rusted 0.7%Si-alloying steel showed a better corrosion resistance than rusted mild steel. Polarization curves demonstrated that Al-/Si-alloying and Al-Si-alloying improved the rest potential of steel at the initial stage; and accelerated the cathodic reduction and anodic dissolution after a rust layer formed on the surfaces of steels. XRD results showed that Al-Si-alloying decreased the volume fraction of $Fe_{3}O_{4}$ and $\alpha-FeOOH$. The recycle of acid accelerated the corrosion of steel at the initial stage. After the rust layer formed on the steel, the leak of rust destabilized the rust layer due to the dissolution of compound containing Al (such as $FeAl_{2}O_{4}$, $(Fe,\;Si)_{2}(Fe,\;Al)O_{4}$). Al-Si-alloying is hence not suitable for improving the anti-corrosion resistance of steel in industrial atmosphere.

• Proceedings of the Korean Fiber Society Conference
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• 2002.04a
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• pp.207-210
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• 2002

PVDF는 측쇄에 C=O기를 갖는 고분자인 PMMA와 PVAc와의 블렌드 및 주쇄에 C=O기를 갖는 poly(1,4-butylene adipate) (PBA)와의 블렌드에서 PVDF의 융점보다 상당히 높은 온도에서 LCST거동을 보이고 있음이 알려져 있다. 그런데 PVDF/PMMA와 PVDF/PVAC 블렌드계에서는 LCST가 고분자의 열분해온도와 유사하여 LCST거동을 실험적으로 관찰하기 어려웠다. 그런데 PVDF/PBA 블렌드계에서는 실험적으로 측정할 수 있을 정도로 LCST가 낮아지긴 하였지만 PBA의 열분해를 완전히 배제하기엔 아직도 높은 온도이다.[1] (중략)

• Corrosion Science and Technology
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• v.22 no.6
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• pp.478-483
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• 2023

This study examined the corrosion behavior of bimetal materials composed of Fe-Ni alloy and Fe-Ni-Mo alloy, both suitable for use in electromagnetic switches. Electrochemical polarization and weight loss measurements revealed that, in contrast to Fe-Ni alloy, which exhibited pseudo-passivity behavior, Fe-Ni-Mo alloy had higher anodic current density, displaying only active dissolution and greater weight loss. This indicated a lower corrosion resistance in the Fe-Ni-Mo alloy. Equilibrium calculations for the phase fraction of precipitates suggested that the addition of 1 wt% Mo may lead to the formation of second-phase precipitates, such as Laves and M₆C, in the γ matrix. These precipitates might degrade the homogeneity of the passive film formed on the surface, leading to localized attacks during the corrosion process. Therefore, considering the differences in corrosion kinetics between these bimetal materials, the early degradation caused by galvanic corrosion should be prevented by designing a new alloy, optimizing heat treatment, or implementing periodic in-service maintenance.

• Journal of the Korean Ceramic Society
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• v.41 no.9
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• pp.642-646
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• 2004

Na$_2$Si$_2$O$_{5}$ added to the solution affects the hydration of 4CaOㆍAl$_2$O$_3$ㆍFe$_2$O$_3$ with calcium sulfate. The reaction between 4CaOㆍAl$_2$O$_3$ Fe$_2$O$_3$and CaSO$_4$ㆍ 2$H_2O$ decrease with increasing amount of Na$_2$Si$_2$O$_{5}$ in solution, owing to low hydraulic reactivity of 4CaOㆍAl$_2$O$_3$ㆍFe$_2$O$_3$by the adsorption of silicate ions on the surface of 4CaOㆍAl$_2$O$_3$ㆍ Fe$_2$O$_3$ particles. The dissolution rate of 4CaOㆍAl$_2$O$_3$ㆍ Fe$_2$O$_3$ particles deceased with the increase of the concentration of silicate ion in solution. When the 4CaOㆍAl$_2$O$_3$ㆍFe$_2$O$_3$ particles was hydrated in gypsum - Na$_2$Si$_2$O$_{5}$ solution, the hydration was retarded and the rate could not discriminate between formation of ettringite and that of monosulfate, and it stopped in high concentration of silicate ions. However, silicate ion did not any effect on the dissolution rate of gypsum.ypsum.

• Proceedings of the KAIS Fall Conference
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• 2008.11a
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• pp.459-462
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• 2008

본 논문에서는 $10K_2O$-30CaO-$60P_2O_5$ mol%를 기본조성으로 하여 Fe, Cu, Zn의 미량성분을 첨가하여 유리를 제조하고 용출 특성을 평가 하였다. 제조된 유리는 미량성분의 첨가량에 따라 유리의 투명도가 변하는 것이 관찰되었다. 용출특성은 측정 4시간 뒤 pH값 증가되는 것으로 16시간 후 pH가 증가하는 것으로 관찰되었다. 여기서 pH의 증가는 염기성산화물이 용출되는 것으로, 감소는 $P_2O_5$구조인 망목형성구조가 붕괴되어지면서 산성이온이 용출되어지는 것으로 판단되어진다. ICP관찰시에는 함량이 증가하면서 K, Ca, P이온의 용출량이 감소되었고, Zn, Cu, Fe이온의 용출량이 증가하는 경향이 관찰되었다.

• Journal of the Korean institute of surface engineering
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• v.51 no.4
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• pp.214-217
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• 2018

Stainless steel grade 430 with a composition of Fe-17%Cr was corroded in $Na_2SO_4$ and ($Na_2SO_4+NaCl$) salts at 800 and at $900^{\circ}C$ for up to 20 h. It corroded mainly to $Cr_2O_3$, along with a small amount of $Fe_2O_3$ and $Fe_3O_4$. The formed oxide scales were neither dense nor compact enough owing to their ensuing dissolution into the salt during corrosion, which facilitated internal corrosion. Corrosion occurred faster at $900^{\circ}C$ than $800^{\circ}C$. NaCl in $Na_2SO_4$ aggravated the scale adherence.

• Proceedings of the Korean Radioactive Waste Society Conference
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• 2015.10a
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• pp.465-466
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• 2015

In this study, different amount of (fe(0)) were dissolve into different strength of phosphoric ($H_3PO_4$) acid and the optimum solubility was observed at 0.89M Fe(0) into 4M of $H_3PO_4$ acid. Different concentration of oxalic acid was added to determine the optimum precipitated condition. The dissolution kinetics of Fe(0) into $H_3PO_4$ acid was investigated at $40-50^{\circ}C$. The optimum Fe-oxalate precipitate was dried and thermal decomposition using DSC-TG was conducted. Approximately 52 wt(%) of oxalic acid was removed at $300^{\circ}C$. Iron oxides such as magnetite and hematite that may be formed on the surface of nuclear waste were also dissolved into the $H_3PO_4$ acid and the optimum solubility for magnetite is 0.005M while that for hematite is 0.02M in 8M $H_3PO_4$ acid, respectively.