• Environmental Engineering Research
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• v.10 no.6
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• pp.269-282
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• 2005

The novel behavior of ferrate(VI) has received an increased attention for its possible applications in various purposes particularly in the treatment of waste/effluent waters. It possess relatively high oxidizing capacity and the reduced ferrate(VI) into Fe(III) again an important and useful precipitant, coagulant, flocculants and likely to be a good adsorbent via the formation of ferric hydroxide for various metal cations. Moreover, the non-toxic effect makes it a 'green chemical' and further enhances its widespread uses in various purposes. Here an attempt has been made to review the applications of ferrate(VI) in the treatment of waste waters and also its possible future applications in the wastewater treatment technology.

• Proceedings of the Korean Society of Soil and Groundwater Environment Conference
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• 2004.09a
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• pp.129-132
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• 2004

A hybrid permeable reactive barriers(hybrid PRBs) composed of Fe(II) PRB, biological PRB and sorptive PRB was investigated to treat groundwater with multiple contaminations. We performed batch, column and pilot tests to determine removal rates and design parameters of each PRB media, and operated two hybrid PRB systems with pilot-scale barriers in series. The pilot test of the hybrid PRB system with the combination of Fe(II), biological media and black shale showed multiple contaminations could be removed in ground water. Nitrate could be treated below 20 mg/L and Cr(VI) was treated down to 0.05 mg/L. TCE was degraded below 0.001 mg/L in system. The hybrid PRB system with a proper combination of PRBs could remediate ground water with multiple contaminations.

• Environmental Engineering Research
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• v.9 no.6
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• pp.249-255
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• 2004

• Bulletin of the Korean Chemical Society
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• v.9 no.2
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• pp.77-80
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• 1988

A suituable choice of supporting electrolyte medium for trace level determinations of chromium(VI) by differential pulse polarography is described. A comparative study suggests that sodium borate buffer is superior to ammonium acetate, ammonium tartrate, and especially to NaF which was recently known to be one of the most proper medium for the purpose. With 0.01 M borate, the best combination of high sensitivity, well-defined base line, and freedom from common interferents was attained. With $5.0{\times}10^{-7}$M Cr(VI), tenfold excesses of Cu(II) and Fe(III), and a five hundred-fold excess of $Cl^-$ do not change the peak current by more than about 1%. And the detection limit was $5.0{\times}10^{-8}$M Cr(VI).

• Asian Journal of Turfgrass Science
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• v.10 no.4
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• pp.297-304
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• 1996

The investigation was performed to reveal the removal rate of metal constituents of litters in a Phragmites communis Miseanthus sacchariflorus, Typha angastata and Seirpas tabernaemontani grasslands in the lake Paldangho. The removal rates of metal constituents are determined by the mathematical models. The removal rates and time required to decay up to a percentage of each metal constituent were calculated using these model. The removal rates of Cu, Fe and Zn were 0.61, 0.58 and 0.79 in Phragmites communis 0.39, 0.47 and 0.68 in Miseanthus saccharflorus; 0.26, 0.09 and 0.23 in Typha angustata: 0.56, 0.27 and 0.67 in Seirpus tabernaemontani respectively. The periods required to reach half time to the stedy state of the removal and accumulation for Cu, Fe and Zn were 1,13,1.19 and 0.79 years in Phragmites communis; 1.79, 1.49 and 1.02 years in Miscanthus sacchariflorus; 2.70, 7.43 and 2.96 years in Typha angustata ; 1.23, 2.58 and 1.04 years in Scirqus tabernaemontani, re-spectively. Key words: Phragmites communis, Miscanthus sacchariflorus, Typha angustata and Scirpus tabernaemontani, lake Paldangho, Removal rate, Cupper, Iron, Zinc.

• Proceedings of the Korea Water Resources Association Conference
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• 2021.06a
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• pp.226-226
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• 2021

Tetractycline은 sulfonamides, penicilines 등과 함께 축산계에서 널리 사용되는 대표적인 항생물질의 한 종류이다. 2011년 사료 내 항생제 투여를 금지한 이후 자가치료 및 예방용으로 사용되고 있으며, 가축의 체내로 투여되는 tetracycline는 주로 분뇨에 포함되어 배출되는데, 강우 등 물 순환에 따라 지표수 및 지하수로 이동하여 미생물에 독성을 일으키거나 내성균이 발생하기도 한다. Tetracycline 등의 항생물질 처리 방식으로 흡착 등 다양한 공정이 제시되고 있다. 본 연구에서는 산화제 중 하나인 ferrate(VI)를 이용하여 tetracycline 분해실험을 수행하였다. ferrate(VI)는 염소산화물 및 H₂O₂에 비해 비교적 강한 산화력을 가지며, 처리 후 발생되는 철염(Fe³⁺)은 독성이 없다는 장점이 있다. Ferrate(VI)는 병원균 제거 등에 효과적인 것으로 알려져 있으며, 다양한 난분해성 물질과 항생물질을 성공적으로 분해하여 그 효과를 입증한 바 있다. 본 연구에서는 자체적으로 제조한 potassium ferrate(VI)를 이용하여 다양한 수중 환경에서 tetracycline를 분해하고, 분해특성 및 중간생성물 연구를 수행하였다. Ferrate(VI)는 염기성 환경에서 tetracycline 분해효율이 가장 높은 것으로 나타났으며, 이는 pH에 따른 tetracycline과 ferrate(VI)의 이온화가 가장 큰 원인인 것으로 판단된다. 특히 ferrate(VI)는 pH가 낮을수록 쉽게 환원되는 특징이 있으며, 염기성으로 갈수록 안정화하여 오래 잔류하므로 이러한 결과가 나타난 것으로 판단된다. 중간생성물 조사 결과, ferrate(VI)와 tetracycline 사이의 분해 메커니즘은 주로 OH 라디칼로 인한 것이 대부분이며, hydroxylation과 amino group에서의 demethylation의 형태로 발생하였다. 이후 추가적인 반응으로 benzene ring이 깨지면서 결과적으로 CO₂ 및 H₂O 등으로 무기물화 되는 것으로 판단된다.

• Journal of Korean Society of Environmental Engineers
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• v.27 no.6
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• pp.657-662
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• 2005

Iron sulfide(FeS) is significantly produced through both abiotic and biotic processes in natural sediments and pore waters. In this study, chromium(VI) reaction with iron sulfide at various initial concentrations and at pH values of 4 and 8 was conducted to better understand the interactions between Cr(VI) and Fe(II) species dissolved from iron sulfide in both the aqueous and solid phases. Also, the removal efficiency of iron sulfide was compared with zero valent iron and other iron bearing oxides such as ${\alpha}-Fe_2O_3$, ${\alpha}-FeOOH$ and $Fe_3O_4$. The Cr(VI) removal rate by iron sulfide was higher at pH 4 than at pH 8 because more dissolved Fe(II) existed at pH 4 than at pH 8. Chromium and iron(oxyhydroxide) could be identified on the iron sulfide surface with transmission microscopy imaging and energy dispersive spectroscopy. The removal capacity of iron sulfide was much higher than zero valent iron and other iron oxide minerals due to the synergic effect of hydrogen sulfide and ferrous iron.

• Journal of Soil and Groundwater Environment
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• v.22 no.4
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• pp.27-32
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• 2017

In this study, a remedial investigation using reductive stabilization was conducted to treat Cr(VI)-contaminated soil. The influences of various operational parameters, including reaction time and the mass of ferrous iron, were also evaluated. The study site was contaminated with a large amount of Cr(III) and Cr(VI), and the selected treatment method was to stabilize Cr(VI) with ferrous iron, which reduced Cr(VI) to Cr(III) and stabilized the chromium, although a greater mass of ferrous iron than the stoichiometric amount was required to stabilize the Cr(VI). However, some Cr(III) re-oxidized to Cr(VI) during the drying process, and addition of a strong reducing agent was required to maintain reducing conditions. With this reducing agent, the treated soil met the required regulatory standard, and the mass of Cr(III) re-oxidized to Cr(VI) was significantly reduced, compared to the use of only Fe(II) as a reducing agent.

• Korean Journal of Environmental Agriculture
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• v.24 no.3
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• pp.203-209
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• 2005

Objective of this research was to assess the effectiveness of the different sources of the zero-valent irons (ZVIs) on the reduction of the toxic Cr(VI) to the nonhazardous Cr(III) in an aqueous solution. The physical and chemical properties of the six ZVIs were determined. Particle size and specific surface area of the ZVIs were in the ranges of $85.55{\sim}196.46{\mu}m\;and\;0.055{\sim}0.091m^2/g$, respectively. Most of the ZVIs contained Fe greater than 98% except for J (93%) and PU (88%). Reduction efficiencies of the ZVI for Cr(VI) reduction were varied with kinds of ZVIs. The J and PU ZVIs reduced 100% and 98% of Cr(VI) in the aqueous solution, respectively, within 3 hrs of reaction. However, PA, F, Sand J1 reduced 74, 65, 29 and 11% of Cr(VI), respectively, after 48 hrs. The pH of the reacting solution was rapidly increased from 3 to $4.34{\sim}9.04$ within 3 hrs. The oxidation-reduction potential (Eh) of the reacting solution was dropped from 600 to 319 mV within 3 hrs following addition of ZVIs to the Cr(VI) contaminated water. The capability of ZVIs for Cr(VI) reduction was the orders of PU > J > PA > F > S > J1, which coincided with the capacities to increase the pH and decrease the redox potentials. Results suggested that the reduction of Cr(VI) to Cr(III) was derived from the oxidation of the ZVI in the aqueous solution.

• Journal of Astronomy and Space Sciences
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• v.18 no.1
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• pp.7-14
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• 2001

Red giant branch shape and the luminosity of horizontal branch on the (V-I)-V CMD are used to derive the metallicity the globular cluster NGC 5053. The metallicities of NGC 5053 derived by SMR method ([Fe/H]=-2.62$\pm$0.07) and the relation between[Fe/H] and $(V-I)_{0.g}$ ([Fe/H]=-2.50) are in good agreement with previously determined values. This result confirms that the morphologies of RGB and HB on the (V-I)-V CMDs can be good indirect photometric metallicity indicators of galactic globular clusters.