• Environmental Engineering Research
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• v.16 no.4
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• pp.187-203
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• 2011

Chlorophenols (CPs) are widely used industrial chemicals that have been identified as being toxic to both humans and the environment. Zero valent iron (ZVI) and iron based bimetallic systems have the potential to efficiently dechlorinate CPs. This paper reviews the research conducted in this area over the past decade, with emphasis on the processes and mechanisms for the removal of CPs, as well as the characterization and role of the iron oxides formed on the ZVI surface. The removal of dissolved CPs in iron-water systems occurs via dechlorination, sorption and co-precipitation. Although ZVI has been commonly used for the dechlorination of CPs, its long term reactivity is limited due to surface passivation over time. However, iron based bimetallic systems are an effective alternative for overcoming this limitation. Bimetallic systems prepared by physically mixing ZVI and the catalyst or through reductive deposition of a catalyst onto ZVI have been shown to display superior performance over unmodified ZVI. Nonetheless, the efficiency and rate of hydrodechlorination of CPs by bimetals depend on the type of metal combinations used, properties of the metals and characteristics of the target CP. The presence and formation of various iron oxides can affect the reactivities of ZVI and bimetals. Oxides, such as green rust and magnetite, facilitate the dechlorination of CPs by ZVI and bimetals, while oxide films, such as hematite, maghemite, lepidocrocite and goethite, passivate the iron surface and hinder the dechlorination reaction. Key environmental parameters, such as solution pH, presence of dissolved oxygen and dissolved co-contaminants, exert significant impacts on the rate and extent of CP dechlorination by ZVI and bimetals.

• Progress in Superconductivity and Cryogenics
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• v.18 no.1
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• pp.28-32
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• 2016

There are a few thousand abandoned metal mines in South Korea. The abandoned mines cause several environmental problems including releasing acid mine drainage (AMD), which contain a very high acidity and heavy metal ions such as Fe, Cu, Cd, Pb, and As. Iron oxides can be formed from the AMD by increasing the solution pH and inducing precipitation. Current study focused on the formation of iron oxide in an AMD and used the oxide for adsorption of heavy metals. The heavy metal adsorbed iron oxide was separated with a superconducting magnet. The duration of iron oxide formation affected on the type of mineral and the degree of magnetization. The removal rate of heavy metal by the adsorption process with the formed iron oxide was highly dependent on the type of iron oxide and the solution pH. A high gradient magnetic separation (HGMS) system successfully separated the iron oxide and harmful heavy metals.

• Korean Journal of Materials Research
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• v.18 no.4
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• pp.218-221
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• 2008

A $Fe(OH)_2$ suspension was prepared by mixing iron sulfate and a weak alkali ammonia solution. Following this, iron oxides were synthesized by passing pure oxygen through the suspension (oxidation). The effects of different reaction temperatures ($30^{\circ}C$, $50^{\circ}C$, $70^{\circ}C$) and equivalent ratios ($0.1{\sim}10.0$) on the formation of iron oxides were investigated. An equilibrium phase diagram was established by quantitative phase analysis of the iron oxides using the Rietveld method. The equilibrium phase diagram showed a large difference from the equilibrium phase diagram of Kiyama when the equivalent ratio was above 1, and single $Fe_3O_4$ phase only formed above an equivalent ratio 2 at all reaction temperatures. Kiyama synthesized iron oxide using iron sulfate and a strong alkali NaOH solution.

• Journal of the Korean Magnetics Society
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• v.7 no.6
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• pp.314-320
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• 1997

We have observed the orientation behavior of acicular iron oxides in magnetic layer of the particular magnetic tape after magnetic paint was coated on polyester film. As results of the static orientation, orientation of iron oxides come to the maximum at the front and the back of orientation magnets, but it was a litter lower at the back than at the front, and it slowly decreases and come to the constant level after passing through the orientation magnets. In case of edge portion to be futher away from center in the coated film, the orientation of iron oxides in magnetic layer come to worse than that of the center. We think it is owing to the shape and the magnetic magnitude of orientation magnets. The results of the dynamic orientation are as follows. As the orientation of iron oxides in the particulated magnetic tape is higher, the output properties of tape come to better than ever. And the orientation of iron oxides can be changed by drying condition, as result, the output properties of tape can be also. Therefore we think the considrations of the design of orientation magnets and the control of drying condition are needed to improve output properties of the particulated magnetic tape.

• The Sea:JOURNAL OF THE KOREAN SOCIETY OF OCEANOGRAPHY
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• v.14 no.3
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• pp.127-133
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• 2009

In order to determine organic carbon oxidation by manganese and iron oxides, six core sediments were obtained in slope and basin sediments of Ulleung Basin in East Sea. The basin sediments show high organic carbon contents (>2%) at the water depths deeper than 2,000 m; this is rare for deep-sea sediments, except for those of the Black Sea and Chilean upwelling regions. In the Ullleung Basin, the surface sediments were extremely enriched by Manganese oxides with more than 2%. Maximum contents of Fe oxides were found at the depth of $1{\sim}4cm$ in basin sediments. However, the high level of Mn and Fe oxides was not observed in slope sediment. Surface manganese enrichments (>2%) in Ulleung Basin may be explained by two possible mechanisms: high organic carbon contents and optimum sedimentation rates and sufficient supply of dissolved Manganese from slope to the deep basin. Reduction rates of iron and manganese oxides ranged from 0.10 to $0.24\;mmol\;m^{-2}day^{-1}$ and from 0.30 to $0.57\;mmol\;m^{-2}day^{-1}$, respectively. In Ulleung Basin sediments, $13{\sim}26%$ of organic carbon oxidation may be linked to the reduction of iron and manganese oxides. Reduction rates of metal oxides were comparable to those of Chilean upwelling regions, and lower than those of Danish coastal sediments.

• Transactions of the Korean hydrogen and new energy society
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• v.17 no.1
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• pp.21-30
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• 2006

[ $M/Fe_2O_3$ ] (M=Rh, Ce and Zr) mixed oxides were prepared using urea method to develop a medium for chemical hydrogen storage by their redox cycles. And their redox behaviors by repeated cycles were studied using temperature programmed reaction(TPR) technique. Additives such as Rh, Ce and Zr were added to iron oxides in order to lower the reaction temperature for reduction by hydrogen and re-oxidation by water-splitting. From the results, concentration of urea used as a precipitant had little effect on particle size and reduction property of iron oxide. TPR patterns of iron oxide consisted of two reduction peaks due to the course of $Fe_2O_3\;{\rightarrow}\;Fe_3O_4\;{\rightarrow}\;Fe$. The results of repeated redox tests showed that Rh added to iron oxide have an effect on lowering the re-oxidation temperature by water-splitting. Meanwhile, Ce and Zr additives played an important role in prevention of deactivation by repeated cycles. Finally, Fe-oxide(Rh, Ce, Zr) sample added with Rh, Ce and Zr showed the lowest re-oxidation temperature by water-splitting and maintained high $H_2$ recovery in spite of the repeated redox cycles. Consequently, it is expected that Fe-oxide(Rh, Ce, Zr) sample can be a feasible medium for chemical hydrogen storage using redox cycle of iron oxide.

• Korean Chemical Engineering Research
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• v.46 no.6
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• pp.1029-1038
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• 2008

Transition-metal-oxide-incorporated hydrotalcites were prepared by hydrothermal reaction of their synthetic mixtures containing precursors of transition metal oxides and their properties of nitrogen dioxide adsorption was investigated. The dispersion of transition metal oxides on the hydrotalcites and the amount and the state of nitrogen dioxide adsorbed on them were examined by using XRD, SEM, XPS, nitrogen adsorption, a gravimetric adsorption system, FT-IR spectroscopy and temperature programmed desorption techniques. Transition metal oxides were mainly incorporated on their surface and the incorporation of iron and nickel oxides to the hydrotalcites increased their adsorption amounts of nitrogen dioxide. The dispersion of iron oxide on the hydrotalcites was effective in increasing the amount of nitrogen dioxide adsorption, while too much amount of iron oxide incorporation reduced the amount of nitrogen dioxide adsorption due to masking of surface basic sites by agglomerated iron oxide. Although the incorporation of iron oxide to the hydrotalcites lowered the adsorption strength of nitrogen dioxide, the incorporation of it with a proper amount enhanced the amount of nitrogen dioxide adsorption and the stability against the hydrothermal treatment.

• Journal of Soil and Groundwater Environment
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• v.21 no.6
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• pp.14-21
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• 2016

This study evaluated the applicability of stabilization of arsenic (As)-contaminated soil with iron (Fe) oxides at the former Janghang smelter site. Three Fe oxides (magnetite, goethite, and hematite) were tested as stabilizing agents to one soil sample collected from the study site. Amendment of 5% of magnetite, goethite, or hematite for one week showed the 64, 58, and 36% of reduction of the SBRC (Solubility/Bioavailability Research Consortium)-extractable (bioaccessible) As, respectively. Duration of stabilization more than one week did not show an additional reduction in SBRC-extractable As. Amendment of 5% of magnetite, which showed the highest As stabilization efficiency, was applied to 24 soil samples collected from the same site for one week, and 72% of reduction in the bioaccessible As was observed. The potential carcinogenic human health risk at the study site caused by As was $1.7{\times}10^{-5}$, which could be reduced to $8.1{\times}10^{-6}$ by the amendment of 5% magnetite for one week.

• Environmental Engineering Research
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• v.14 no.2
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• pp.134-139
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• 2009

In this study, oxidation of As (III) as well as removal of total arsenic by adsorbents coated with single oxides or multi-oxides (Fe (III), Mn (IV), Al (III)) was investigated. In addition, multi-functional properties of adsorbents coated with multi-oxides were evaluated. Finally, application of activated carbon impregnated with Fe or Mn-oxides on the treatment of As (III) or As (V) was studied. As (V) adsorption results with adsorbents containing Fe and Al shows that adsorbents containing Fe show a greater removal of As (V) at pH 4 than at pH 7. In contrast adsorbents containing Al shows a favorable removal of As (V) at pH 7 than at pH 4. In case of iron sand, it has a negligible adsorption capacity for As (V) although it contains 217.9 g-Fe/kg-adsorbent, Oxidation result shows that manganese coated sand (MCS) has the greatest As (III) oxidation capacity among all metal oxides at pH 4. Oxidation efficiency of As (III) by IMCS (iron and manganese coated sand) was less than that by MCS. However the total removed amount of arsenic by IMCS was greater than that by MCS.

• Resources Recycling
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• v.7 no.4
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• pp.76-80
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• 1998

In order to establish the ICP composition analysis system of the compotes which have been producing and using the domestic iron oxides, the Sectional Committee of Iron Oxides had organized an analysis working team. which carried out the component analysis of several samples and den discussed about thou analysis results through 1 year. At the 1st meeting, the component deviation was reduced. At the 3rd meeting, the deviation range if each company was reduced below ${\pm}$20% and it means to be improved on an analysis level with Japaness steel companies.