• 한국환경농학회지
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• 제42권3호
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• pp.253-258
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• 2023

In the environment, chromium often exists in a highly mobile and toxic form of Cr(VI). Therefore, the reduction of Cr(VI) to less toxic Cr(III) is considered an effective remediation strategy for Cr(VI)-contamination. In this study, the biological reduction of hexavalent chromium was examined at the concentrations of 0.01 mM, 0.1 mM, and 1 mM Cr(VI) by the dissimilatory metal-reducing bacterium, Shewanella sp. HN-41 in the presence of ferric-citrate. With the relatively condensed cell densities, the aqueous phase Cr(VI) was reduced at the proportions of 42%, 23%, and 31%, respectively for the 0.01 mM, 0.1 mM, and 1 mM Cr(VI) incubations, while Fe(III)-citrate was reduced at 95%, 88%, and 73%, respectively. Although the strain HN-41 was not considered to reduce Cr(VI) as the sole electron acceptor for anaerobic metabolism in the preliminary experiment, it has been presumed that outer-membrane c-type cytochromes such as MtrC and OmcA reduced Cr(VI) in the presence of ferric-citrate as the electron acceptor. Since this study indicated the potential of relatively high cell density for Cr(VI) reduction, it might propose a bioremediation strategy for Cr(VI) removal from contaminated waters using engineered systems such as bioreactors employing high cell growths.

• Bulletin of the Korean Chemical Society
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• 제27권5호
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• pp.694-698
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• 2006

A method has been described for the chemical speciation, preconcentration and determination of Cr(III) and Cr(VI) species in filtered tannery waste waters by flame atomic absorption spectrometry using ion-exchange resins. Amberlite IR-120($H^+$) strongly acidic cation exchanger and Amberlite IRA-410($CI ^-$) strongly basic anion exchanger resins were used for the separation and preconcentration of Cr(III) and Cr(VI) species, respectively. Optimum condition for preconcentration and speciation was obtained by testing pH of sample and eluent, flow rates of sample and eluent, amount of resins, volume of sample and eluents, and effect of foreign ions. The recommended method has been successfully applied for the preconcentration and determination of chromium species in the dissolved phase of waste water samples collected from a tannery waste water treatment plant in Kayseri, Turkey. The detection limits achieved were 0.73 $\mu$g/L for Cr(III) and 0.81 $\mu$g/L for Cr(VI). Recovery studies showed 99% for Cr(III) and 98% for Cr(VI), for samples spiked with single species.

• 한국방사성폐기물학회:학술대회논문집
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• 한국방사성폐기물학회 2004년도 Proceedings of the 4th Korea-China Joint Workshop on Nuclear Waste Management
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• pp.245-256
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• 2004

The extraction of three kinds of amido podands, N,N,N'N'-tetrabutyl-3-oxa-pentanedi- amide (TBDGA), N,N,N'N'-tetra-isobutyl-3-oxa-pentanediamide(TiBDGA) and N,N,N'N'-tetra- butyl-3,6-dioxa-oct-anediam- ide(TBDOODA) on U(VI),Pu(IV), Am(III), Eu(III) and other metal ions is studied in nitric acid solutions. 40%octanol-kerosene is chosen as diluents to eliminate third phase and emulsion. TBDGA and TiBDGA show extraction selectivity to An(III) and Ln(III) much higher than to U(VI) and Pu(IV). Fe, Ru and Mo is poorly extracted by the three kinds of amid podands in 2~3mol/L $HNO_3$ solutions. Aiming to eliminate interface crude when using simulated HLLW solution in the system of 0.2mol/L TBDGA/Octanol＋kerosene, acetohydroxyamic acid was adapted. Distribution ratio of zirconium was decreased when adding acetohydroxyamic acid in aqueous solution, and interface crude disappeared as mixing extractant with HLLW. The counter-current extraction test is carried out in a set of miniature mixer-settler, with 0.2mol/L TBDGA/ 40% octanol-kerosene as extractant to separate U(VI), Pu(IV), Am(III) and Eu(III) from simulated high level liquid waste(HLLW) solution. In battery A, lanthanides and actinides are coextracted into organic phase with the recovery of 99.98% for U(Ⅵ), >99.99% for Pu(IV), and >99.99% for Am(III) and Eu(III) respectively. In battery R1, 99.99% U, 86.2% Pu and a part of Am or Eu are stripped into aqueous phase by 0.2mol/L acetohydroxyamic acid (AHA) in 0.01mol/L $HNO_3$ solution. In battery $R_2$, Am, Eu and remained Pu are completely back-extracted by 0.2mol/L AHA. This separation process contains no salt reagent, and it is not necessary to dilute HLLW feed.

• 대한화학회지
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• 제57권6호
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• pp.703-711
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• 2013

In the present investigation, kinetic studies of oxidation of formic acid with and without catalyst and promoter in aqueous acid media were studied under the pseudo-first order conditions [formic acid]T ${\gg}[Cr(VI)]_T$ at room temperature. In the 1,10-phenanthroline (phen) promoted path, the cationic Cr(VI) phen complex is the main active oxidant species undergoes a nucleophilic attack by the substrate to form a ternary complex which subsequently experiences a redox decomposition through several steps leading to the products $CO_2$ and $H_2$ along with the Cr(III) phen complex. The anionic surfactant (i.e., sodium dodecyl sulfate, SDS) and neutral surfactant (i.e., Triton X-100, TX-100) act as catalyst and the reaction undergo simultaneously in both aqueous and micellar phase with an enhanced rate of oxidation in the micellar phase. Whereas the cationic surfactant (i.e., N-cetyl pyridinium chloride, CPC) acts as an inhibitor restricts the reaction to aqueous phase. The observed net enhancement of rate effects has been explained by considering the hydrophobic and electrostatic interaction between the surfactants and reactants. The neutral surfactant TX-100 has been observed as the suitable micellar catalyst for the phen promoted chromic acid oxidation of formic acid.

• 한국결정성장학회지
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• 제28권3호
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• pp.135-139
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• 2018

본 연구에서는 HVPE 성장법을 이용하여 사파이어 기판 위에 알파 갈륨옥사이드를 성장시키며 VI/III 비의 변화에 따른 효과를 확인하였다. 성장된 알파 갈륨옥사이드의 표면은 평평하고 crack 없이 성장되었다. 성장된 갈륨옥사이드의 광학적 특성을 분석하기 위해 투과율을 측정하고 광학 밴드갭을 얻었다. 광학 밴드갭은 약 5.0 eV로 나타났고 VI/III 비가 증가함에 따라 비례하여 증가하는 결과를 보여주었다. 이론적 광학 밴드갭에 가장 근접한 VI/III 비가 23인 조건에서 성장된 알파 갈륨옥사이드의 결정성을 확인하기 위해 HR-XRD를 이용하여 FWHM을 측정하였고 이를 바탕으로 전위밀도를 계산하였을 때 나선형 전위밀도는 $1.5{\times}10^7cm^{-2}$, 칼날 전위 밀도는 $5.4{\times}10^9cm^{-2}$로 계산되었다.

• 한국표면공학회지
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• 제23권2호
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• pp.1-10
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• 1990

Metal-Organic Vapor Phase Epitaxy (MOVPE) is an epitaxial process utilizaing ane or more of organometallice as reactnte to grow compound semicond semiconductror layers. MOVPE is basically a cold wall process in which reactants are delivered without reacting with each other to the heated substrate where reactants are thermally decomposed to from compound semiconductors through chemical reaction. Since reactants are delivered as gas phase and the formation of the single crystal compunds depends on the thermal decomposition of the reactants, details of MOVPE relies on the hydrodynamics and pyroltsis and chemical reation of reactants inside on reaction chamber. It has been demonstrated that MOVPE is capable of growing virtually all of the III-V, II-VI and IV-VI compound semiconductrs, fabricating ultrathin epilayers, for ming abrupt hetrointerfaces with monolayer transition width, and is suitable for multi-wafer operation yilding a high throghtput. Overiew of reactror componts and layer, characteristics, and status of MOVPE are discussed.

• 한국항공우주학회지
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• 제36권4호
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• pp.315-320
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• 2008

본 논문은 상용유동해석코드인 Fluent를 이용하여 NREL(National Renewable Energy Laboratory) Phase VI 로터에 대한 공력특성을 연구하였다. 해석 결과는 NREL/NASA Ames 풍동 시험결과와 비교하였다. 풍력터빈로터의 반경방향에 대해 속도의 변화에 따른 압력분포를 비교하였다. 계산된 결과는 저속일 때 실험결과와 잘 일치 하였지만 고속일 때 블레이드의 suction side에서 실험결과와 잘 일치하지 않았다. 2기의 풍력터빈간의 거리가 풍력터빈 로터지름의 10배일 때 후류의 영향을 고려한 후방 풍력터빈 로터의 공력해석을 수행하였다.

• 상하수도학회지
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• 제36권3호
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• pp.167-175
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• 2022

수용액에서 EBT의 분해는 pH, Ferrate (VI) 투입량, 초기 농도, 수용액 온도 등 다양한 변수의 조건에서 연구되었다. 최대 분해 효율은 pH 7.0에서 95.42%가 달성되었으며, 이 실험 조건에서 얻은 kapp 값은 872.87 M^-1s^-1 이었다. EBT 분해율은 Ferrate (VI)의 투입량이 증가함에 따라 증가하였으며 EBT 초기 농도가 감소함에 따라 EBT 분해의 초기 속도 상수가 증가하였다. 또한 EBT의 분해율은 온도가 10℃에서 45℃에 도달할 때까지 수용액의 온도에 따라 증가하였으며 이 실험조건에서 활성화 에너지 값은 EBT 분해에 대해 11.9 kJ/mol의 값이 도출되었다. 따라서 분해 실험의 결과는 Ferrate (VI)가 수용액상에서 EBT를 효과적으로 분해시킬 수 있음을 보여주고 있다.

• Bulletin of the Korean Chemical Society
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• 제31권10호
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• pp.2813-2818
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• 2010

A novel method was developed for the speciation of chromium in natural water samples based on homogeneous liquid-liquid extraction and determination by flame atomic absorption spectrometry (FAAS). In this method, Cr(III) reacts with a new Schiff's base ligand to form the hydrophobic complex, which is subsequently entrapped in the sediment phase, whereas Cr(VI) remained in aqueous phase. The Cr(VI) assay is based on its reduction to Cr(III) by the addition of sodium sulfite to the sample solution. Thus, separation of Cr(III) and Cr(VI) could be realized. Homogeneous liquid-liquid extraction based on the pH-independent phase-separation process was investigated using a ternary solvent system (water-tetrabutylammonium ion ($TBA^+$)-chloroform) for the preconcentration of chromium. The phase separation phenomenon occurred by an ion-pair formation of TBA and perchlorate ion. Then sedimented phase was separated using a $100\;{\mu}L$ micro-syringe and diluted to 1.0 mL with ethanol. The sample was introduced into the flame by conventional aspiration. After the optimization of complexation and extraction conditions such as pH = 9.5, [ligand] = $1.0{\times}10^{-4}\;M$, [$TBA^+$] = $2.0{\times}10^{-2}\;M$, [$CHCl_3$] = $100.0\;{\mu}L$ and [$ClO_4$] = $2.0{\times}10{-2}\;M$, a preconcentration factor (Va/Vs) of 100 was obtained for only 10 mL of the sample. The relative standard deviation was 2.8% (n = 10). The limit of detection was sufficiently low and lie at ppb level. The proposed method was applied for the extraction and determination of chromium in natural water samples with satisfactory results.

• 분석과학
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• 제6권3호
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• pp.329-334
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• 1993

형성시킨 Mo(VI)의 킬레이드이온과 이온쌍을 만들어 유기용매에로 상승추출시켜 자연수 중 극미량의 몰리브덴[Mo(VI)]을 분리 정량하는 방법을 해수에 응용하였다. pH 2.0과 4.0에서 anthranilic acid를 가해 Cu(II)와 Fe(III), Zn(II)을 침전시켜 그들의 방해를 제거한 해수시료 100mL를 분액 깔때기에 취하였다. pH를 4.6으로 조절한 시료에 0.01M alizarin red S 1.0mL를 가하여 Mo(VI)-ARS의 킬레이트이온을 형성시킨 다음 aliquat-336을 0.6% 되게 녹인 chloroform 10mL를 가해 30초 정도 격렬하게 흔들어 모든 킬레이트이온이 이온쌍을 형성하도록 하였다. 30분간 방치하여 두 상이 완전히 분리되면 chloroform층을 받아서 520nm에서 흡광도를 측정하여 검정곡선법으로 Mo(VI)을 정량하였다. 이상의 과정에서 추출조건인 용액의 pH, alizarin red S와 aliquat-336의 가해 주는 양, 흔들어 주고 방치하는 시간 등과 공존 이온들의 방해와 제거방안에 대해서 검토하였다. 실제 시료인 동해와 황해 해수의 분석에 응용하였으며, 이들 시료에 Mo(VI)을 일정량 가하여 분석한 회수율은 모두 85% 이상으로 본 방법을 해수 중 Mo(VI)의 분석에서도 정량적임을 확인하였다.