• 자원리싸이클링
• /
• 제7권3호
• /
• pp.3-10
• /
• 1998

모의폐액으로 제조한 50ppm의 코발트이온을 Fe(III) 및 Al(III)의 응집제와 sodium lauryl sulfate의 계면활성제를 사용하여 흡착 교질 포말부선법으로 제거하였다. 용액의 pH, 계면활성제 농도, Fe(III) 및 Al(III) 농도, 공급기체의 유속 등을 변수로 하여 실험한 결과, Fe(III)를 응집제로 사용한 경우 초기 코발트이온농도 50ppm, pH 8.5, 공급기체유속 $70mell$/min, 제거시간 15분 등의 조건에서 99.8%의 제거율을 나타내었다. 코발트 이온 제거에 앞서 모의폐액에 35% $H_2O_2$를 첨가하여 폐액을 전처리하였다. 그 결과, 최적 pH 및 처리 후 잔존용액의 pH가 낮아졌고, 넓은 범위의 pH에서 높은 제거율을 나타내었다. Fe(III) 50 ppm을 사용하여 코발트이온과 공침시킨 후 20ppm의 Al(III)를 첨가한 결과, Fe(III) 또는 Al(III)를 각각 단독으로 사용하였던 경우에 비하여 제거 가능한 pH 범위가 더욱 더 확대되었다. 이 현상은 zeta potential 의 증가 및 공침효과의 상승요인으로 추측되었다. $NO_3^-$, $SO_4^{2-}$, $Na^+$, $Ca^{2+}$를 첨가하여 외부이온의 영향을 관찰하였으며, $SO_4^{2-}$가 0.1M 함유된 코발트용액을 Fe(III) 및 Al(III)를 사용하여 처리한 결과 제거효율은 99%를 나타내었다.

• Corrosion Science and Technology
• /
• 제4권2호
• /
• pp.45-50
• /
• 2005

A 3% NaCl solution of 1 $dm^3$ circulated with 1.5 $dm^3/min$ by a pump for 24 h in the presence of magnetic field. An iron plate immersed in a $100cm^3$ of test solution for 24 h. The rest potential and pH on surface fixed after 3 h. Containing 0~120 ppm of Fe(II) ion, the dissolution in the magnetically treated solution rose comparing with that in the non-magnetically treated solution. The dissolution amount reached to maximum at 50 ppm, then fixed in the non-magnetically treated solution. When Fe(II) ion existed in the magnetically treated solution, dissolution accelerated a little. In the non-magnetic treated solution containing 10~125 ppm of Fe(III) ion existed, the dissolution accelerated. The dissolution amounts reached to maximum at 50 ppm, then decreased from maximum value. In the magnetically treated solution, the dissolution amounts reached to minimum until 50 ppm, then increased from minimum value. The dissolution amounts affected larger with increasing of magnetic flux density. Fe(II), Fe(III) ions and magnetic treatment affected to formation of $Fe(OH)_2$ and/or $Fe_3O_4$ films. The magnetically treated effects memorized about one month.

• 한국식품저장유통학회지
• /
• 제6권1호
• /
• pp.115-120
• /
• 1999

This study was carried out to investigate the effect of Pine needle extract on lipid oxidation and free radical reaction in iron sources reacted with active oxygen species. The results were summarized as follow; The pine needle extracts didn`t show a distinct effect on reduction of lipid oxidation if the iron ion didn`t exist in oil emulsion. The pine needle extracts played role as a strong chelating agents to bind iron ion if Ferrous iron(Fe\ulcorner) exist in oil emulsion. Ferric iron(Fe) was lower effect than Ferrous iron(Fe) on free radical reaction in oil emulsion. And also, the Fe\ulcorner reacted with pine needle extract did not show distinct effect on free radical reaction, compared to Fe\ulcorner reacted with pine needle extract. And also, Pine needle extracts reacted with H\ulcornerO\ulcorner were tended to show a low oxygen scavenging ability in case of H\ulcornerO\ulcorner only was existed, compared to those of H\ulcornerO\ulcorner + Fe\ulcorner complex. Pine needle extracts were the most powerful Fe\ulcorner binding agents, compared to other strong synthetic antioxidants such as EDTA and DTPA.

• 한국재료학회지
• /
• 제32권4호
• /
• pp.230-236
• /
• 2022

The formation behavior of a passive state film on the surface of STS304 in electrolytic solution was analyzed to determine its metallic ion composition. The properties of passive state films vary depending on the Fe and Cr ions in the electrolytic solution. It was observed that the passive state film surface became flat and glossy as the concentration of Fe and Cr ions in the electrolytic solution increased. The corrosion resistance property of the passive state film was proportional to the amount of Fe and Cr in the electrolytic solution. An initial passive state film with high Fe concentration was formed on the surface of STS304 during early electrolytic polishing. Osmotic pressure of Fe ions occurs between the passive state film and electrolytic solution due to the Fe ion concentration gradient. The Fe in the passive state film is dissolved into the electrolyte, and Cr fills up the Fe ion vacancies. As a result, a good corrosion-resistant floating film was formed. The more Fe ions in the electrolytic solution, the faster the film is formed, and as a result, a flat passive state film containing a large amount of Cr can be formed.

• 한국자기학회지
• /
• 제8권1호
• /
• pp.6-12
• /
• 1998

플라즈마 이온주입 장치를 이용하여 $\alpha$-Fe foil에 질소 이온을 주입하여 질화철 결정상을 만들었으며, 이때 질소 이온 주입시간을 15분(FEN15)과 30분 (Fe30)으로 처리되었다. 오제 전자 분광법(Auger electron spectroscopy : AES)을 이용하여 측정한 주입된 질소 이온의 깊이는 사편 FeN15와 FeN30에서 각각 12000$\AA$과 40000$\AA$으로 나타난다. 진동 시편 자력계(vibrating sample magnetometer : VSM)측정결과 as-implanted 각각의 시편은 포화자화 값이 순수한 $\alpha$-Fe foil 보다 증가되었으며, 이는 $\alpha$'-Fe8N 또는 $\alpha$'-Fe16N2의 결정구조가 그원인으로 판단된다. 따라서 본 연구는 플라즈마 이온주입 방법으로 제작된 질화철에서 부분적인 $\alpha$'또는 $\alpha$'의 졀정구조 형성 가능성을 확인할 수 있었다.

• Journal of Radiation Protection and Research
• /
• 제40권2호
• /
• pp.87-91
• /
• 2015

We have employed X-ray photoelectron spectroscopy (XPS) technique to examine the combined effects of low-energy electron (LEE) irradiation and $Fe^{3+}$ ion on DNA damage. pBR322 plasmid DNA extracted from E. coli ER2420 was used for preparing DNA-$Fe^{3+}$ sample. The C1s XPS spectra were scanned for LEE-irradiated and LEE-unirradiated samples and then curve-fitted. For the samples with LEE irradiation only or with Fe ion only, no significant changes from pure DNA samples were observed - a single effect of either $Fe^{3+}$ ion or LEE irradiation did not cause a significant damage. However, when these two components were combined, the DNA damage was increased quite significantly, compared to the sum of DNA damages caused by $Fe^{3+}$ ion and by LEE irradiation independently. This observation is consistent with our previous results [Radiat. Res. 177, 775 (2012)] which was done using gel-electrophoresis technique. Partial interpretation of the observed spectrum peaks was also attempted.

• 한국재료학회:학술대회논문집
• /
• 한국재료학회 1998년도 추계학술발표강연 및 논문개요집
• /
• pp.44-44
• /
• 1998

• Journal of Electrochemical Science and Technology
• /
• 제2권4호
• /
• pp.193-197
• /
• 2011

The influences of the thickness and microstructure of Fe layer on the electrochemical performances of Fe/Si multilayer thin film anodes were investigated. The Fe/Si multilayer films were prepared by electron beam evaporation, in which Fe layer was deposited with/without simultaneous bombardment of Ar ion. The kinetics of Li insertion/extraction reactions in the early stage are slowed down with increasing the thickness of Fe layer, but such a slowdown seems to be negligible for thin Fe layers less than about $500{\AA}$. When the Fe layer was deposited with ion bombardment, even the $300{\AA}$ thick Fe layer significantly suppress Li diffusion through the Fe layer. This is attributed to the dense microstructure of Fe layer, induced by ion beam assisted deposition (IBAD). It appears that the Fe/Si multilayer films prepared with IBAD show good cyclability compared to the film deposited without IBAD.

• Bulletin of the Korean Chemical Society
• /
• 제33권11호
• /
• pp.3625-3628
• /
• 2012

Fluorescent organic molecules that respond to changes in the $Fe^{2+}$ concentration with selectivity to other abundant di-valent metal ions will offer the ability to understand the dynamic fluctuations of the $Fe^{2+}$ ion in interesting media. The use of 6-Br-ppmbi, derived from 2-pyridin-2-yl-benzimidazole, for metal ion-selective fluorescence recognition was investigated. Screening of the main group and transition metal ions showed exclusive selectivity for $Fe^{2+}$ ions even in the presence of competing metal ions. In addition, the requirement for low concentrations of probe molecules to detect certain amounts of $Fe^{2+}$ ions make this sensor unique compared to previously reported $Fe^{2+}$ ion sensors.

• 한국분말재료학회지
• /
• 제19권1호
• /
• pp.13-18
• /
• 2012

This study has been performed on the full density sintering of Fe nanopowder and the surface hardening by plasma ion nitriding. The Fe sintered part was fabricated by pressureless sintering of the Fe nanopowder at $700^{\circ}C$ in which the nanopowder agglomerates were controlled to have 0.5-5 ${\mu}m$ sized agglomerates with 150 nm Fe nanopowders. The green compact with 46% theoretical density(T.D.) showed a homogeneous microstructure with fine pores below 1 ${\mu}m$. After sintering, the powder compact underwent full densification process with above 98%T.D. and uniform nanoscale microstructure. This enhanced sintering is thought to be basically due to the homogeneous microstructure in the green compact in which the large pores are removed by wet-milling. Plasma ion nitriding of the sintered part resulted in the formation of ${\gamma}$'-$Fe_4N$ equilibrium phase with about 12 ${\mu}m$ thickness, leading to the surface hardening of the sintered Fe part. The surface hardness was remarkably increased from 176 $H_v$ for the matrix to 365 $H_v$.