• 한국지하수토양환경학회지:지하수토양환경
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• 제14권2호
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• pp.26-32
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• 2009

본 연구에서는(Fe$^{3+}$+chelating agent)/H$_2$O$_2$ 공정 [Fe(III) 1mM, ocalate 6mM, H$_2$O$_2$ 3%, pH 6]과 UV/(Fe$^{3+}$+chelating agent)/H$_2$O$_2$ 공정 [UV dose 17.4kWh/L, Fe(III) 1mM, oxalate 6mM, H$_2$O$_2$ 1%, pH6]에서 BTEX(benzene, toluene, ethylbenzene, xylene)를 분해하기위해 다양한 착제를 토입, 그 분해효율을 비교하였다. 착제의 종류는 catechol, NTA, gallic, acetyl acetone, succinic, acetate, EDTA, citrate, malonate, 그리고 oxalate,총 10가지 종류의 착제를 사용하였으며, 그 중,acetate를 착제로 사용한 경우, 가장 높은 분해효율을 나타내었다. 또한, UV를 조사한 경우, 모든 착제에 대한 BTEX의 분해효율이 UV를 조사하지 않은 (Fe$^{3+}$+chelating agent)/H$_2$O$_2$ 공정의 분해효율보다 높은 것으로 나타났다. 또한BTEX와 무연 휘발유의 첨가제로 사용되고 있는 MTBE(methl tert-butylether)의 혼합복합물(각각의 농도는 200mg/L)에 대해서도 acetate를 착제로 사용한 UV/(Fe$^{3+}$+chelating agent)/H$_2$O$_2$공정에서 높은 분해효율을 보였다. 이 경우, BTEX는 반응시간 180분 만에 완전 분해되었으며, MTBE의 경우, 85%의 분해효율을 보였다. 이러한 실험 결과는 acetate를 착제로 사용한 UV/(Fe$^{3+}$+chelating agent)/H$_2$O$_2$공정은 BTEX 분해효율뿐만 아니라, BTEX와 MTBE복합오염물의 분해효율도 증가시킬수 있음을 입증하고 있다.

• 한국지하수토양환경학회지:지하수토양환경
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• 제16권6호
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• pp.19-26
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• 2011

In this research, soil analysis and adsorption were conducted, and compared with the water quality of bank filtration and river in terms of TS, TDS, SS, $NH_4$-N, $NO_3$-N, $NO_2$-N, Fe, Mn, BOD and $KMnO_4$ consumption for the development of bank filtration in Gimhae city. Analysis of soil showed high levels of Fe (470 mg/kg), Mn (80 mg/kg) and $NH_4$-N (15 mg/kg). Also, adsorption coefficient values (k and 1/n) were 0.00159 and 0.8714, respectively. This implies that the adsorption of the soil depends on organic matter. Water qualitiy of the river and the bank filtration revealed that the concentrations of TS and TDS almost didn't change but the concentration of SS decreased 84% through the bank filtration. $NH_4$-N in the bank filtration was detected more than 1 mg/L which might be due to agricultural activities in the research area. $NO_3$-N was close to the detection limit owing to the removal by the adsorption. $KMnO_4$ consumption and BOD of the river were decreased by the bank filtration 250% and 350%, respectively, while Fe and Mn were significantly increased by the bank filtration.

• Environmental Engineering Research
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• 제13권3호
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• pp.131-135
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• 2008

In this study, Fe(VI) was employed as a multi-functional agent to treat the simulated industrial wastewater contaminated with Cu(II)-EDTA through oxidation of EDTA, decomplexation of Cu(II)-EDTA and subsequent removal of free copper through precipitation. The decomplexation of $10^{-4}\;M$ Cu(II)-EDTA species was performed as a function of pH at excess concentration of Fe(VI). It was noted that the acidic conditions favor the decomplexation of Cu(II)-EDTA as the decomplxation was almost 100% up to pH 6.5, while it was only 35% at pH 9.9. The enhanced degradation of Cu(II)-EDTA with decreasing the pH could be explained by the different speciation of Fe(VI). $HFeO_4^-$ and $H_2FeO_4$, which are relatively more reactive than the unprotonated species $FeO_4^{2-}$, are predominant species below neutral pH. It was noted that the decomplexation reaction is extremely fast and within 5 to10 min of contact, 100% of Cu(II)-EDTA was decomplexed at pH 4.0. However, at higher pH (i.e., pH 10.0) the decomplexation process was relatively slow and it was observed that even after 180 min of contact, maximum ca 37% of Cu(II)-EDTA was decomplexed. In order to discuss the kinetics of the decomplexation of Cu(II)-EDTA, the data was slightly fitted better for the second order rate reaction than the first order rate reaction in the excess of Fe(VI) concentration. On the other hand, the removal efficiency of free Cu(II) ions was also obtained at pH 4.0 and 10.0. It was probably removed through adsorption/coagulation with the reduced iron i.e., Fe(III). The removal of total Cu(II) was rapid at pH 4.0 whereas, it was slow at pH 10.0. Although the decomplexation was 100% at lower pH, the removal of free Cu(II) was relatively slow. This result may be explicable due to the reason that at lower pH values the adsorption/coagulation capacity of Fe(III) is greatly retarded. On the other hand, at higher pH values the decomplexation of Cu(II)-EDTA was partial, hence, slower Cu(II) removal was occurred.

• 한국전기전자재료학회:학술대회논문집
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• 한국전기전자재료학회 2002년도 춘계학술대회 논문집 센서 박막재료 반도체재료 기술교육
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• pp.74-77
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• 2002

Ferroelectric Random Access Memory(FRAM) and MEMS applications require noble metal or refractory metal oxide electrodes. In this study, Ru thin films were etched using $O_2$+10% $CF_4$ plasma in an inductively coupled plasma(ICP) etching system. The etch rate of Ru thin films was examined as function of rf power, DC bias applied to the substrate. The enhanced etch rate can be obtained not only with increasing rf power and DC bias voltage, but also with small addition $CF_4$ gas. The selectivity of $SiO_2$ over Ru are 1.3. Radical densities of oxygen and fluorine in $CF_4/O_2$ plasma have been investigated by optical emission spectroscopy(OES). The etching profiles of Ru films with an photoresist pattern were measured by a field emission scanning electron microscope (FE-SEM). The additive gas increases the concentration of oxygen radicals, therefore increases the etch rate of the Ru thin films and enhances the etch slope. In $O_2$+10% $CF_4$ plasma, the etch rate of Ru thin films increases up to 10% $CF_4$ but decreases with increasing $CF_4$ mixing ratio.

• Journal of Magnetics
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• 제18권3호
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• pp.230-234
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• 2013

The $Ni_{0.5}Zn_{0.5}Fe_2O_4$ nanoparticles about 30 nm were prepared using sol-gel method with metal nitrates dissolved in 2-methoxyathanol. The concentrations of the metal nitrates are adjusted from 0.1 to 0.75 M in order to study the influence on the structural and magnetic properties. The structure and morphology characterization revealed that the crystallinity was improved and the nanoparticle size was increased with the nutrition solution concentrations up to 0.5 M. Degraded crystallinity together with decreased nanoparticle size were observed for concentration of 0.75 M. The saturation magnetization at room temperature reached maximum at 0.5 M, which can be explained by considering the crystallinity and size effect.

• 자원환경지질
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• 제48권3호
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• pp.261-271
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• 2015

본 총설 논문에서는 다양한 급성독성법을 이용하여 중금속, 나노입자, 중금속 오염 토양에 의한 영향 평가 결과를 소개하였다. 평가는 씨앗발아, 생물발광, 효소활성 및 유전자 변이 평가법을 이용하였으며, 오염물 종류 및 방법에 따라 상이한 민감도를 보였다. 씨앗의 경우에는 상추(Lactucus)와 알타리무(Raphanus)가 대체적으로 높은 민감도를 보였다. 단일 금속 노출에서는 일반적으로 As(III)가 높은 독성을 나타내었다. As(III) 1 mg/L 조건에서 높은 유전자변이(MR=5.1)가 관찰되었다. 혼합 중금속에 대한 영향은 명확한 경향을 찾기 어려웠지만, 씨앗 발아의 경우에는 상승 효과가 보편적으로 관찰되었다. 중금속 오염 토양에 대한 평가에서는 시료별 총중금속 농도와 독성 영향 간의 상관성을 예측하기는 어려웠다. 일반적으로 나노입자의 씨앗발아에 근거한 영향은 다음의 순서로 조사되었다: CuO > ZnO > NiO > $TiO_2$, $Fe_2O_3$, $Co_3O_4$. 특히 $TiO_2$, $Fe_2O_3$와 $Co_3O_4$는 최대 노출 농도 1,000 mg/L 농도에서도 뚜렷한 영향을 나타내지 않았다. 다양한 독성 생물검정법에 대한 통합 자료는 향후 다양한 오염물 기초 독성평가에 유용하게 사용할 수 있을 것이다.

• 한국신재생에너지학회:학술대회논문집
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• 한국신재생에너지학회 2008년도 추계학술대회 논문집
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• pp.230-233
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• 2008

The vanadium rich ash of petroleum coke can give a slagging problem during because of the high melting point of $V_2O_3$. For continuous removal of the slag, petroleum coke is often mixed with coal, and the viscosity of the mixed slag is an important property, determining the gasification temperature. The viscosities of the mixed slag from various mixing ratios of petroleum coke and a bituminous coal were investigated. When mixed with a crystalline coal slag, $T_{cv}$ was increased at a higher the coke content in the mixed feed. When the $V_2O_3$ concentration was greater than 4.5%, it was difficult to get accurate measurements of $T_{cv}$. The SEM/EDX analyses of the cooled slag revealed that the major crystalline phase was anorthite, and $T_{cv}$ should be related to the formation temperature of anorthite. The SEM/EDX analyses also showed that, at low concentrations of vanadium, part vanadium formed a crystalline phase with Al-Si-Ca-Fe, and the rest remained in the glassy phase, suggesting that vanadium existed as a slag component at the low viscosity region. At a high concentration, vanadium forms a phase with Ca, and the Ca-V phase was separated from the slag phase, and formed a layer above the slag. FeO in petroleum coke also played an important role determining viscosity: at high temperatures, increased FeO lowered the viscosity, but as it formed a spinel phase, the depletion of FeO in the slag resulted in a higher viscosity.

• Environmental Engineering Research
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• 제25권2호
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• pp.186-196
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• 2020

Pillared clays with Zr and Fe/Cu/Zr polycations have been prepared from natural clays found in large deposits of Kazakhstan and assessed as catalysts for the catalytic wet peroxide oxidation (CWPO), using 4-nitrophenol (4-NP) as model compound. The performance of the catalysts was followed by measuring the concentration of 4-NP, H₂O₂ and the total organic carbon (TOC), considering C_4-NP = 5 g L^-1, $C_{H_2O_2}$ = 17.8 g L^-1, C_cat = 2.5 g L^-1, initial pH = 3.0 and T = 50℃. At those selected conditions, the pillared clays showed higher activity than natural clays in the CWPO of 4-NP. The conversion of the model pollutant was complete when Fe/Cu/Zr-PILCs were used, with the TOC removal reaching 78.4% after 24 h with the best Fe/Cu/Zr-PILC. The H₂O₂, 4-NP and TOC time-evolution was well described by a kinetic model based on TOC lumps in three blocks, considering the initial TOC (corresponding to 4-NP), the production of oxidizable intermediates and the formation of refractory products.

• Bulletin of the Korean Chemical Society
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• 제33권9호
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• pp.3009-3016
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• 2012

This study evaluated the use of iron-impregnated SBA-15 (Fe/SBA-15) as a catalyst for the oxidative degradation of persistent phenol analogues, such as 2-chlorophenol (2-CP), 4-chlorophenol (4-CP), 2-nitrophenol (2-NP), 4-nitrophenol (4-NP) and 2,4,6-trichlorophenol (2,4,6-TCP) in water. The oxidation reactions were carried out with reaction time, concentration of the phenols, amount of the catalysts, reaction temperature, pH of the reaction mixture as the process variables with or without using hydrogen peroxide as the oxidizing agent. The conversion achieved with Fe/SBA-15 at 353 K for 2-CP, 4-CP, 2-NP, 4-NP, 2,4,6-TCP was 80.2, 71.2, 53.1, 62.8, 77.3% in 5h with a reactant to $H_2O_2$ mole ratio of 1:1, and 85.7, 65.8, 61.9, 63.7, 78.1% in the absence of $H_2O_2$, respectively. The reactions followed pseudo first order kinetics. The leachability study indicated that the catalyst released very little iron into water and therefore, the possibility of secondary pollution is negligible.

• 대한화학회지
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• 제37권10호
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• pp.874-880
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• 1993

산소를 수용체로 하여 $H_2O_2$를 생성하는 산화효소인 glucose oxidase (GO) 와 alcohol oxidase (AO)를 이용하여 glucose와 ethanol에 대한 분광학적 효소분석법과 전기화학적 효소분석법을 연구하였다. Glucose에 대한 정량분석의 경우 GO 반응에서 생성된 $H_2O_2$를 peroxidase를 사용하여 $K_4Fe(CN)_6$에 반응시키고 그 결과 생성된 $K_3Fe(CN)_6$의 흡광도를 418 nm에서 측정하거나 Ag/AgCl (포화 KCl) 기준전극에 대하여 -55 mV를 부하시킨 유리질 탄소전극에서 $K_3Fe(CN)_6$의 확산전류를 측정하였다. 전류법 측정이 분광광도법 측정보다 1/1000 정도 더 낮은 농도까지 검출할 수 있었으며 직선성을 갖는 농도 범위도 10배 더 연장되었다. Ethanol에 대한 정량분석의 경우 $K_3Fe(CN)_6$가 AO에 의하여 순간적으로 소거되었으므로 AO 반응만을 이용하여 $H_2O_2$의 생성속도를 +0.900 V에서 측정하거나 용존 $O_2$의 감소속도를 -0.500 V에서 전류법으로 측정하였다.