• 한국지하수토양환경학회:학술대회논문집
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• 한국지하수토양환경학회 2002년도 총회 및 춘계학술발표회
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• pp.250-253
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• 2002

Remediation of groundwater using zero valent iron filings has received considerable attention in recent years. However, zero valent iron is gradually transformed to iron(III) oxides at permeable reactive barriers, so the reduction of iron(III) oxides can enhance the longevity of the reactive barriers. In this study, microbial reduction of Fe(III) was performed in anaerobic condition. A medium contained nutrients similar to soil solution. The medium was autoclaved and deoxygenated by purging with 99.99% $N_2$ and pH was buffered to 6, while the temperature was regulated as 2$0^{\circ}C$. Activity of iron reducing bacteria were not affected by chlorinated organics but affected by iron(III) oxide. Although perchloroethylene(PCE) was not degraded with only ferric oxide, PCE was reduced to around 50% with ferric oxide and microorganism. It shows that reduced iron can dechlorinate PCE.

• 자원환경지질
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• 제54권2호
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• pp.299-308
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• 2021

광산 활동에서 비롯된 Fe(II)은 광산 배수를 따라 지표의 산화 환경에 노출되어 다양한 Fe(III)-산화수산화물로 침전된다. 대표적인 Fe(III) 침전 광물 중 하나인 페리하이드라이트는 결정도가 매우 낮아 비표면적이 크기 때문에, 중금속 및 다른 오염물질을 흡착하기에 용이하다. 페리하이드라이트는 자연 환경에서 열역학적으로 좀더 안정적인 침철석으로 전이된다. 페리하이드라이트에서 침철석으로 전이되는 동안 일어나는 중금속의 거동을 예측하기 위해서 산성광산배수에서 일어나는 페리하이드라이트에서 침철석으로의 전이와 이와 연관된 중금속의 유동성에 대한 정보는 중요하다. 광물 전이와 중금속 거동을 분석하기 위해 흥진태맥 석탄광의 산성광산배수 정화 시설의 코어 시료에 대하여 X-선 회절 분석(XRD), 화학 분석, 통계 분석이 시행되었다. XRD 결과는 페리하이드라이트가 코어 시료 상단에서 하단으로 점차 침철석으로 전이되었음을 보여주었다. 화학 분석 결과 코어시료에서 As의 상대적 농도는 배수에 비하여 매우 높아 As가 철옥시수산화물에 강하게 흡착 되었거나 공침되었을 가능성이 큼을 지시한다. 상관 분석 결과 또한 As와 Fe의 높은 친화도를 보여주어, 철광물이 침전하는 동안 As가 광산 배수에서 쉽게 제거될 수 있음을 나타냈다. 코어 시료에서 깊이가 깊어질수록 Fe에 대한 As, Cd, Co, Ni, Zn의 농도비는 대체로 감소하여, 광물 전이 시 배수 내 이들의 농도를 증가시킬 수 있음을 나타냈다. 이와 반대로 Fe에 대한 Cr의 농도는 깊이가 증가할수록 증가하였는데 이 것은 chromate과 철광물과의 화학결합과 페리하이드라이트와 침철석의 표면 전하로 인한 것으로 생각된다.

• Bulletin of the Korean Chemical Society
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• 제14권4호
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• pp.439-444
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• 1993

The aerobic oxidation of the Fe(II) complex of 1,4,8,11-tetraazacyclotetradecane, [Fe(cyclam)$(CH_3CN)_2](ClO_4)_2$, in MeCN in the presence of a few drops of $HClO_4$ leads to low spin Fe(III) species [Fe(cyclam)$(CH_3CN)_2](ClO_4)_3$. The Fe(III) cyclam complex is further oxidized in the air in the presence of a trace of water to produce the deep green binuclear bismacrocyclic Fe(II) complex $[Fe_2(C_{20}H_{36}N_8)(CH_3CN)_4](ClO_4)_4{\cdot}2CH_3CN$. The Fe(II) ions of the complex are six-coordinated and the bismacrocyclic ligand is extensively unsaturated. $[Fe_2(C_{20}H_{36}N_8)(CH_3CN)_4](ClO_4)_4{\cdot}2CH_3CN$ crystallizes in the monoclinic space group $P2_1/n$ with a= 13.099 (1) ${\AA}$, b= 10.930 (1) ${\AA}$, c= 17.859 (1) ${\AA}$, ${\beta}$= 95.315 $(7)^{\circ}$, and Z= 2. The structure was solved by heavy atom methods and refined anisotropically to R values of R= 0.0633 and $R_w$= 0.0702 for 1819 observed reflections with F > $4{\sigma}$ (F) measured with Mo K${\alpha}$ radiation on a CAD-4 diffractometer. The two macrocyclic units are coupled through the bridgehead carbons of ${\beta}$-diimitie moieties by a double bond. The double bonds in each macrocycle unit are localized. The average bond distances of $Fe(II)-N_{imine}$, $Fe(II)-N_{amine}$, and $Fe(II)-N_{MeCN}$ are 1.890 (5), 2.001 (5), and 1.925 (6) ${\AA}$, respectively. The complex is diamagnetic, containing two low spin Fe(II) ions in the molecule. The complex shows extremely intense charge transfer band in the near infrared at 868 nm with ${\varepsilon}$= 25,000 $M^{-1}cm^{-1}$. The complex shows a one-electron oxidation wave at +0.83 volts and two one-electron reduction waves at -0.43 and-0.72 volts vs. Ag/AgCl reference electrode. The complex reacts with carbon monoxide in $MeNO_2$ to form carbonyl adducts, whose $v_{CO}$ value (2010 $cm^{-1}$) indicates the ${\pi}$-accepting property of the present bismacrocyclic ligand.

• 자원환경지질
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• 제20권1호
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• pp.61-75
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• 1987

The Daejang mine is one of the representatives of Cu-Pb-Zn-(Ag) vein deposit related genetically to late Cretaceous granitoid in Korea. Sericite from an alteration halo of the mine yielded a K-Ar date of $95{\pm}3.5Ma$. Based on macrostructures of vein filling, three major mineralization stages (I, II and III) are distinguished by tectonic breaks. Major ore constituents are arsenopyrite, pyrite, pyrrhotite, sphalerite, chalcopyrite, galena, boulangerite, with small amounts of Ag-bearing tetrahedrite, pyrargyrite, native bismuth, marcasite, siderite, ankerite, gudmundite and calcite. Characteristic feature of each mineralization stage and compositional variation of sphalerite and arsenopyrite are discussed in relation to the genetic environments. The FeS contents of sphalerites are 20.5~14.9 mole % in stage I, 17.9~11.9 mole % in stage IIA, 17.0~9.2 mole % in stage IIB, and 6.9~4.7 mole % in stage III. Their results are indicative of decreasing FeS contents during mineralization process in sphalerite coexisting with sulfur-rich sulfide assemblages, such as monoclinic pyrrhotite and pyrite, and is agreement with the conclusions shown by Scott and Kissin(1973). The composition of arsenopyrite decrease also in As content from stage I to stage III, and the compositional variation correlate with position of the associated minerals in the paragenesis. Temperature and pressure of the mineralization are determined as $250{\sim}430^{\circ}C$ and 4.0~0.3kb respectively, based on the chemistry of the minerals.

• 한국세라믹학회지
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• 제22권1호
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• pp.5-10
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• 1985

The effect of calcium lignosulfonate (CLS) on the early hydration characteristics for clinker minerals was investigated. In the presence of CLS and unsufficient gypsum The hydration of $C_3$A lowered CLS adsorption to form ettrin-gite and the residual CLS in the liquid phase accelerated the solubility of C4AF hydration. As the result unreacted $Fe^{3+}$ in the liquid phase would be precipitated gelatinously on $C_3$ hydrates and the hydration of $C_3$ could be retarded. But by addition of optimum gypsum into the cement with CLS the presence of $Fe^{3+}$ in the liquid phase were lowered and $C_3$ hydration would be normallized.

• 한국염색가공학회지
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• 제14권1호
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• pp.34-42
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• 2002

In order to investigate the light fastness of Korean knotweed extract, the concentrate were prepared and dyed to silk fabric under the various conditions, such as kinds of mordants, methods of mordanting, and the dye concentration. After the deed fabrics were irradiated for several hours, the color differences and K/S values were measured. Additionally, the light fastness of Korean knotweed extracts and Emodin in liquid solution was compared. The light fastness of silk fabrics deed with Korean knotweed extract was improved by the Introduction of Fe-mordant, but the surface colors on the dyed fabrics shaded into reddish and dark yellow by 80hours irradiation. Color difference of fabrics were increased wish concentrations of Korean knotweed extracts. So inconsistent fading behaviour was observed. Color difference of dyed fabrics increased remarkably at the early stage of fading and became slowly down except for Fe-mordanted fabric. Absorbance of Korean knotweed extracts and Emodin in liquid solution were extremely decreased with concentrations of colorants, so inconsistent fading behaviour was observed too.

• 천문학회지
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• 제42권4호
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• pp.93-103
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• 2009

This article reports the spectral behavior of CH Cygni, using data obtained in October 2005 and June 2006. In these epochs, CH Cygni showed emission lines of H I, Fe II, [Fe II], [O III], [N II], [Ne III] and [S II]. Many of these lines were more enhanced since 2004. The underlying M-type spectrum was removed to get the intrinsic emission profile, and the resulting profiles were deconvoluted into several Gaussian components. Also, the radial velocities for all the lines that appeared in these spectra of CH Cygni were measured. The resultant lines were compared with each other and with those obtained in 2004; the findings are explained in terms of an accretion disk and jets.

• 한국생물공학회:학술대회논문집
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• 한국생물공학회 2002년도 생물공학의 동향 (X)
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• pp.390-393
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• 2002

BTEX가 함유된 groundwater에 에탄올이 첨가된 경우 토양 미생물에 의한 BTEX의 분해는 에탄올이 존재하지 않는 경우에 비해 크게 낮아짐을 알 수 있었다. 이는 토양내 미생물이 에탄올을 우선 이용하며, 따라서 토양내 산소와 mineral의 결핍을 야기하여 BTEX의 분해가 느려짐에 기인한다. 전자수용체로 Fe(III), nitrate, sulfate를 groundwater에 첨가한 경우, BTEX의 분해도는 크게 증가하였으며, sulfate의 효과가 가장 높았다.

• 한국환경보건학회지
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• 제19권4호
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• pp.33-37
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• 1993

The problem for the removal of phosphorus increased due to reasons like eutrophication control. However its removal and operating criteria were not well developed. This study was made for enhanced removal of P by iron contactor by intermittent aeration activated sludge process. Experiment was conducted to find the effects of organic substance load and HRT, nutrient removal efficiency. When applied organic substance load and HRT, II &III reactor were good treatment efficient while come from Fe of iron contactor. Release of phophorus from II &III reactor sludge under anaerobic condition was low. As the process developed, the content of released ionized Fe from iron contactor increased. In addition, the rate of phosphorus removal became accelerating, and the removed sludge was stabilized in the existence of insoluble status.

• 대한화학회지
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• 제9권1호
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• pp.41-44
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• 1965

7-Nitroso-8-hydroxyquinoline-5-sulfonate의 Fe(II)錯鹽의 性質을 700$m{\mu}$, $26^{\circ}C$에서 分光光度法으로 調査하였다. 이 錯鹽은 pH6.0에서 가장 큰 吸光度를 나타내며 熱安定度도 대단히 좋다. Ligand나 Fe(III)의 還元에 使用한 hydroxylamine이 過剩으로 存在할때 에도 錯鹽의 生成에 影響을 주지 않는다. 錯鹽의 組成을 몰比法과 連續變化法으로 調査한 結果, 金屬과 ligand의 몰比는 1:3이였다. 檢量線은 實驗한 濃度範圍內에서 Beer의 法則에 따른다.