• Bulletin of the Korean Chemical Society
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• 제30권11호
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• pp.2577-2583
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• 2009

Presented are the formation of iron oxide layers on evaporator tubes in an actual fossil power plant operated under all volatile treatment (AVT) condition and an experimental simulation of iron oxide formation in the presence of ferrous and ferric ions. After actual operations for 12781 and 36326 hr in the power plant, two iron oxide layers of magnetite on the evaporator tubes were found: a continuous inner layer and a porous outer layer. The experimental simulation (i.e., artificial corrosion in the presence of ferrous and ferric ions at 100 ppm level for 100 hr) reveals that ferrous ions turn the continuous inner oxide layer on tube metal to cracks and pores, while ferric ions facilitate the production of porous outer oxide layer consisting of large crystallites. Based on a comparison of the oxide layers produced in the experimental simulation with those observed on the actually used tubes, we propose possible routes for oxid layer formation schematically. In addition, the limits of the proposed corrosion routes are discussed in detail.

• 한국세라믹학회지
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• 제48권2호
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• pp.117-120
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• 2011

In this study, the redox state of iron in sodium silicate glasses was varied by changing the melting conditions, such as the melting temperature and particle size of iron oxide. The oxidation states of the iron ion were determined by wet chemical analysis and UV-Vis spectroscopy methods. Iron commonly exists as an equilibrium mixture of ferrous ions, $Fe^{2+}$, and ferric ions $Fe^{3+}$. In this study, sodium silicate glasses containing nanoparticles of iron oxide (0.5% mol) were prepared at various temperatures. Increase of temperature led to the transformation of ferric ions to ferrous ions, and the intensity of the ferrous peak in 1050 nm increased. Nanoparticle iron oxide caused fewer ferrous ions to be formed and the $\frac{Fe^{2+}}{Fe^{3+}}$ equilibrium ratio compared to that with micro-oxide iron powder was lower.

• 한국환경과학회:학술대회논문집
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• 한국환경과학회 2003년도 가을 학술발표회 발표논문집
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• pp.319-321
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• 2003

This research was carried out to evaluate the removal efficiencies of CODcr and colour for the dyeing wastewater by ferrous solution in Fenton process. The results showed that COD was mainly removed by Fenton coagulation, where the ferric ions are formed in the initial step of Fenton reaction. On the other hand colour was removed by Fenton oxidation rather than Fenton coagulation. The removal mechanism of CODcr and colour was mainly coagulation by ferrous ion, ferric ion and Fenton oxidation. The removal efficiencies were dependent on the ferric ion amount at the beginning of the reaction. However the final removal efficiency of COD and colour was in the order of Fenton oxidation, ferric ion coagulation and ferrous ion coagulation. The reason of the highest removal efficiency by Fenton oxidation can be explained by the chain reactions with ferrous solution, ferric ion and hydrogen peroxide.

• 한국환경과학회지
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• 제13권11호
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• pp.987-991
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• 2004

The purpose of this research is to evaluate the removal efficiencies of COD$\_$Cr/ and color for the dyeing wastewater by the different dosages of ferrous solution and H$_2$O$_2$ in Fenton process. In the case of H$_2$O$_2$ divided dosage for the Fenton's reagent 7:3 of H$_2$O$_2$ was more effective than 3:7 to remove COD$\_$Cr/ and color. The results showed that COD$\_$Cr/ was mainly removed by Fenton coagulation, where the ferric ions are formed in the initial step of Fenton reaction. On the other hand color was removed by Fenton oxidation rather than Fenton coagulation. The removal mechanism of COD$\_$Cr/ and color was mainly coagulation by ferrous ion, ferric ion and Fenton oxidation. The removal efficiencies were dependent on the ferric ion amount at the beginning of the reaction. However, the final removal efficiency of COD$\_$Cr/ and color was in the order of Fenton oxidation, ferric ion coagulation and ferrous ion coagulation. The reason of the highest removal efficiency by Fenton oxidation can be explained by the chain reactions with ferrous solution, ferric ion and hydrogen peroxide.

• 분석과학
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• 제35권5호
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• pp.218-227
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• 2022

A simple and fast throughput flow injection (FI) system with a merging-zone technique was designed to determine ferrous and ferric in an aqueous solution. The method is based on the direct reaction of ferrous with a Bathophenanthroline reagent (Bphen) in acidic media. The forming red complex absorbs light at 533 nm. All conditions of the flow injection system were investigated. The analytical curve of ferrous was linear in the range of 0.07 to 4 mg/L with an r² value of 0.9968. The detection and quantification limits were 0.02 and 0.04 mg/L, respectively. The molar absorptivity and Sandell's sensitivity were 4.0577 × 10⁶ L/mol cm and 25 × 10^-5 ㎍/cm², respectively. The homemade valve was low-cost with high repeatability (n = 7) at an RSD of 1.26 % and zero dead volume. The values of the dispersion coefficient were 2.318, 2.022, and 1.636 for the concentrations of 0.2, 1, and 3 mg/L, respectively. The analysis throughput of the designed flow injection unit was 57 sample per hour.

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

• 한국가금학회지
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• 제16권1호
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• pp.17-22
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• 1989

난백의 열광수성을 순화시키기 위하여 각종금속염(Fe$^{2＋}$, Fe$^{3+}$ , $Al^{3+}$ , Cu$^{2＋}$)을 첨가하고 가훈처리($60^{\circ}C$, 5분간) 전후 난백의 기능성을 검토하였으며 알루미늄염(Al$^{3+}$ )이 첨가된 난백의 pH에 대한효과도 검토하였다. 금속염의 첨가에 의해 가열처리 전후 난백의 탁도는 대체로 증가하였으나 알루미늄염의부가시 탁도의 변화가 가장 작았다. 난백의 기포력은 금속염의 첨가에 의해 전반적으로 증가하였으며 Fe$^{3+}$ 의 첨가효과가 가장 컸다. 특히 가열처리 후 난백의 기포력은Fe$^{3+}$ , Al/ sup 3＋/ 및 Cu$^{2＋}$의 첨가에 의해 크게 증가되었다. 기포안정성의 경우 열처리 전에는 Fe$^{3+}$ , Al/ sup 3＋/의 첨가효과가 있었으나 열처리 후에는 Fe$^{3+}$ 와 Al/ sup 3＋/의 첨가가 효과적이었다. 한편 알루미늄염을 첨가한 난백을 pH 7 -10의 범위에서 가열처리한 결과 pH 7-8.5 범위에서는 탁도 및 기포성의 변화가 크지 않았고 pH 9이상에서는 탁도와 기포성은 낮아졌으나 기포안정성은 향상되었다. 난백액에 Salmonella typhimurium을 $10^{6}$ cells/$m\ell$수준으로 접종 후 $60^{\circ}C$, 5분간의 가열처리 결과 pH에 상관없이 모두 사멸되었다.

• 한국균학회지
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• 제21권3호
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• pp.157-164
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• 1993

1. 표고버섯중 광감응성 mitochondrial $F_1-ATPase$는 $Fe^{3+},\;Fe^{2-}$ 및 $Mg^{2+}$ 이온에 의하여 각각 활성화 되었으나 5.0 mM $Fe^{3+}$ 이온에 의한 상대활성도는 대조구에 비하여 107% 증가시켰다. 2 $Mg^{2+}$ 존재하에서 $Fe^{3+}$ 및 $Fe^{2-}$ 각 이온 농도효과는 모두 효소의 활성을 증가시켰으나 0.1 mM $Mg^{2+}$과 5.0 mM $Fe^{3+}$ 이온의 공존하에서 170%를 증가시켜 $Mg^{2+}$ 이온에 의한 상승작용을 보였다. 3. 0.1 mM $Mg^{2+}$와 0.1 mM $Fe^{2+}$ 존재하에서 $Fe^{3+}$ 이온농도효과는 그 농도가 5.0 mM일 때 168%의 활성도 증가를 보여 $Fe^{2-}$ 이온공존효과는 없었다. 4. 이 효소는 $Mg^{2+}$ 및 $Fe^{3+}$ 이온에 의하여 활성화되는 특성을 가지고 있으며 활성금속이온 존재하에서 측정한 최적 pH 빛 온도는 각각 7.5 및 $66^{\circ}C$였다.

• 한국식품과학회지
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• 제53권6호
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• pp.785-791
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• 2021

다양한 유산균들이 생체에 유익한 영향을 주는 프로바이오틱스로 제시되고 있는 가운데, 본 연구에서는 L. kimchicus, L. lactis, L. casei, L. plantarum, LGG 및 Leu. mesenteroides 등 유산균 6종을 선별하여 균주별 nitrate의 환원과 nitrite의 소거, 그리고 철 이온에 대한 환원활성을 분석하였다. 사용된 6종의 유산균 중, 5종의 균주에서 72시간 배양시간 동안 nitrate에 대한 환원현상이 나타나지 않았으나, L. kimchicus는 nitrate의 환원을 통해 과량의 nitrite를 생성했다. 한편, nitrite 소거활성은 균주별로 상당한 차이를 보였으며, 특히 L. kimchicus는 nitrate와의 반응과 마찬가지로 가장 높은 소거능을 나타내어 반응시간과 균수에 따른 급격한 배지 중 nitrite 수준 감소를 유도하였다. Ferric ion의 ferrous ion으로의 환원에 있어서도 L. kimchicus가 다른 5종의 균주에 비해 420-1500배의 높은 활성을 보였다. L. kimchicus의 환원활성은 멸균처리 균주나 균체 용해물에서는 거의 발현되지 않아 생균의 대사능력에 의한 것으로 나타났다. 이러한 L. kimchicus의 활성은 프로바이오틱스로서의 효과뿐만 아니라, 관련 환원활성에 의한 NO 등 유용 포스트바이오틱스 대사물에 의한 효과도 기대할 수 있을 것으로 판단된다.

• Bulletin of the Korean Chemical Society
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• 제27권4호
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• pp.489-494
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• 2006

Goethite, hematite, magnetite and synthesized iron oxide are used as catalysts for Fenton-type oxidation of phenol. The synthesized iron oxides were characterized by X-ray diffraction (XRD), BET, X-ray photoelectron spectroscopy (XPS), and electron paramagnetic resonance (EPR). The catalytic activity of these materials is classified according to the observed rate of phenol oxidation. The effectiveness of the catalysts followed the sequence: ferrous ion > synthesized iron oxide >> magnetite hematite > goethite. According to these results, the most effective iron oxide catalyst had the structure similar to natural hematite. The surface oxidation state of the catalyst was between magnetite and hematite (+2.5 ~ +3.0). Phenol degraded completely in 40 min at neutral pH (pH = 7). Soluble ferric and ferrous ions were not detected in the filtrate from Fenton reaction solution by AAS. The formation of hydroxyl radicals was confirmed by EPR.