• Journal of the Korean Chemical Society
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• v.46 no.6
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• pp.509-514
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• 2002

A method to determin Fe(II) and Fe(III) ion in aqueous solution by chemiluminescence method using a stopped flow system has been studied. The method is based on the increased chemiluminescence intensity with the addition of Fe(III) ion to a solution of lucigenin and hydrogen peroxide. The effects of KOH concentration, flow rate of reagents, $H_2O_2$ concentration and citric acid concentration used for the masking of Fe(II) ion on the chemilu-minescence intensity have been investigated. The calibration curve for total Fe was linear over the range from 1.0${\times}$$10^{-6}$ M to 1.0${\times}$$10^{-4}$M, coefficient of correlation was 0.996 and the detection limit was 1.0${\times}$$10^{-7}$M under the optimal exper-imental conditions of 4.0 M, 2.0 M, 3.5 mL/min for the concentration of $H_2O_2,$ KOH and flow rate of reagents, respec-tively. The calibration curve for Fe(Ⅲ) was linear over the range from 1.0${\times}$$10^{-6}$M to 1.0${\times}10^{-4}$ M, the coefficient of correlation was 0.997 and the detection limit was 5.0${\times}$$10^{-7}$M under the optimal experimental conditions.

• Journal of the Korean Crystal Growth and Crystal Technology
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• v.8 no.4
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• pp.525-531
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• 1998

A series of $LiNbO_3$ single crystals were grown by the Czochralski method from a congruent melt, a congruent melt with 0.05 mol% $Fe_2O_3$, a congruent melt with 6 wt.% $K_2O$ and a congruent melt with 6 wt.% $K_2O$ and 0.05 mol% $Fe_2O_3$ respectively. The growth of $LiNbO_3$ crystal from a congruent melt 6 wt.% $K_2O$ leads to nearly stoichiometric specimens. This is established by studying the following properties; XRD patterns, temperature dependences of the phase transition temperature, energy of the fundamental absorption edge, the shape of the absorption band of the $OH^-$vibration and linewidths of the ESR of $Fe_{Li}^{3+}$.

• Journal of the Korean Magnetics Society
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• v.5 no.4
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• pp.281-286
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• 1995

In order to study the effect of additives $SiO_{2}$ on the magnetic properties of hexaferrite sheet magnet, we used X-ray diffractometer, Mossbauer spectrometer, and VSM magnetometer. We have prepared $Ba_{0.25}Sr_{0.75}Fe_{12}O_{19}$ green sheets by the Dr. Blade method. Most of samples have a magnetoplurnbite crystal structure of typical M-type hexaferrite. The lattice parameters are found not to be affected by the addition of $SiO_{2}$. ${\alpha}-Fe_{2}O_{3}$ phase develops above $SiO_{2}$ 2.0 wt.%. Isomer shifts indicate that the valence of Fe ions is trivalent. Curie temperatures decrease slightly with increasing $SiO_{2}$ concentrations. It means that the $Si^{4+}$ subsitution for 12k-site $Fe^{3+}$ has an effect on the superexchange interactions Fe-O-Fe, which change the distance and the angle between cations and anions. It was suggested that ${\alpha}-Fe_{2}O_{3}$ phase results from the excessive Fe produced by subsituting $Si^{4+}$ for $Fe^{3+}$. Based upon the results of $Ba_{0.25}Sr_{0.75}Fe_{12}O_{19}$ added with $SiO_{2}$, we concluded that $H_{c}$, $M_{s}$ and $M_{r}$ depend more strongly on the microstructure chracteristics than on the cation substitution.

• Resources Recycling
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• v.31 no.1
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• pp.12-20
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• 2022

The smelting reduction of spent lithium-ion batteries results in metallic alloys containing Co, Cu, Fe, Mn, Ni, and Si. A process to separate metal ions from the sulfuric acid leaching solution of these metallic alloys has been reported. In this process, ionic liquids are employed to separate Fe(III) and Cu(II). In this study, D2EHPA and Cyanex 301 were employed to replace these ionic liquids. Fe(III) and Cu(II) from the sulfate solution were sequentially extracted using 0.5 M D2EHPA with three stages of cross-current and 0.3 M Cyanex 301. The stripping of Fe(III) and Cu(II) from the loaded phases was performed using 50% (v/v) and 60% (v/v) aqua regia solutions, respectively. The mass balance results from this process indicated that the recovery and purity percentages of the metals were greater than 99%.

• Clean Technology
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• v.18 no.1
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• pp.89-94
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• 2012

In this study, we investigated the activity of Pd and Pt supported on acidic Fe-ZSM5 supports for selective catalytic oxidation of ammonia ($NH_3$-SCO). Among the catalysts, Pt/Fe-ZSM5 catalyst exhibited superior $NH_3$-SCO activity to Pd/Fe-ZSM5 catalyst. We also tested Pt/Fe-ZSM5 catalysts with different Fe loading using ion-exchange method to prepare Fe-ZSM5 supports, which resulted in the increased catalytic performance with smaller Fe content: $NH_3$ was oxidized completely at low temperature ($250^{\circ}C$). The physicochemical properties of Fe-ZSM5 were investigated to figure out the relationship between the characteristics of the catalysts and the catalytic activity on $NH_3$-SCO by Inductively coupled plasma-atomic emissions spectrometer (ICP-AES), $N_2$ sorption, X-ray diffraction (XRD), temperature programmed desorption of $NH_3$ ($NH_3$-TPD) technique.

• Journal of the Korean Magnetics Society
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• v.17 no.1
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• pp.47-50
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• 2007

[ $ZnCr_2O_4$ ] shows geometrically frustrated magnet. Recently, $CoCr_2O_4$ has been investigated for multiferroic property and dielectric anomalies by spin-current model. Polycrystalline $CoCr_2O_4$ and $CoCrFeO_4$ compounds was prepared by wet-chemical process. Crystallographic and magnetic properties of $CoCr_2O_4$ and $CoCrFeO_4$ were investigate by using the x-ray diffractometer(XRD), vibrating sample magnetometer(VSM), superconducting quantum interference device magnetometer(SQUID), and $M\"{o}ssbauer$ spectroscopy. The crystal structure was found to be single-phase cubic spinel with space group of Fd3m. The lattice constants of $CoCr_2O_4$ and $CoCrFeO_4$ $a_0$ were determined to be 8.340 and 8.377 ${\AA}$, respectively. The ferrimagnetic transition temperature for the both samples were observed at 97 K and 320 K. The $M\"{o}ssbauer$ absorption spectra at 4.2 K show that the well developed two sextets are superposed with small difference of hyperfine field($H_{hf1}=507\;and\;H_{hf2}=492\;kOe$). Isomer shift values($\delta$) of the two sextets are found to be 0.33 and 0.34 mm/s relative to the Fe metal, respectively, which are consistent with the high spin $Fe^{3+}$ charge state.

• Journal of the Korean Crystal Growth and Crystal Technology
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• v.9 no.5
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• pp.447-453
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• 1999

Congruent $LiNbO_3$ crystals with doped Mg and codoped with Mn or Fe were grown by the Czochralski method. It is known that the physical properties of $LiNbO_3$ depend strongly on the addition of Mg and transition metals. This is established by studying the following properties; XRD patterns, the phase transition temperature, energy of the fundamental absorption edge, the shape of the absorption band of the $OH^-$ vibration and lines of the ESR of $Fe^{3+},\; Mn^{2+}$. The position of the UV absorption edge and the shape and peak point of the absorption band of the $OH^-$ vibrational band changed monotonously up to a critical concentration of $Mg^{2+}$ ions. The mechanism of the incorporation of Mg ions changes at this concentration. The transition temperature was estimated by measuring the dielectric temperature behavior up to $1230^{\circ}C$ in a frequency range of 100Hz to 10MHz. EPR of $Mn^{2+}\;and\; Fe^{3+}$ ions were employed to investigated the Mg doping effects in the $LiNbO_3$ crystal. The increase of linewidths and the asymmetry of signals were observed in all crystals. New signals of $Fe^{3+}$ arising from the new centers were observed I the heavily Mg-doped crystals.

• Journal of the Korean Chemical Society
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• v.53 no.3
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• pp.368-376
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• 2009

In this study we investigated and tried to understand problems monitored in an experiment on reactivity of metals in chemistry I. Three problems were discussed. First, the reason that aluminium plate does not react with other metal ions such as zinc, iron and copper was studied and the way to overcome this problem was suggested. Second, the reason that the bubbles were generated when FeS$O_4$(aq) and Zn(s) react was discussed. Third, the precipitates which appeared in the reaction of FeS$O_4$(aq) and Zn(s) were identified. Through reference study and experimental investigation, we could reach the following results. First, aluminium could not react with other metal ions due to the surface oxide layer that is formed very fast and prevents aluminium from reacting with metal ions in solution. This problem could be overcome by allowing a competing reaction of acid and aluminium during the reaction of aluminium and metal ions. Second, the observed bubbles were identified to be hydrogen gas, produced by the reaction between metals and hydronium ion in the solution. Third, black precipitates that were produced on the surface of zinc plate and exhibited magnetic property were characterized to be $Fe_3O_4$(s), and brown precipitates that were produced in the solution phase were to be $Fe_2O_3$(s) by the analysis of X-ray photoelectron spectra.

• Journal of the Korean earth science society
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• v.26 no.3
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• pp.297-304
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• 2005

Serpentinites in Chungnam area are mainly composed of serpentines. Serpentines of olivine origin consist of pseudomorphs of olivines and show mesh textureen closed with magnetites along the boundaries of serpentine crystals. In some serpentinites, serpentinization is occurred in crystal boundaries and/or cracks of olivines and pyroxenes which are relict minerals of dunite and harzburgite. On the process from olivine to serpentine, Mg ions are greatly decreased and Si ions are greatly increased, and $Fe^{2+}\;and\;Fe^{3+}$ ions are a little decreased. But, on the process from pyroxene to serpentine, Si ions are greatly decreased and Mg ions are greatly increased. Magnetites around the serpentine crystals were formed from the iron which had been left out through this serpentinization process of olivine. Serpentinization from the original rocks such as dunite and harzburgite in Chungnam area was occurred by various waters affected after formation of original rock, and particularly by metamorphic water in the metamorphic conditions ranging from green schist facies to granulite facies through amphibolite facies.

• Proceedings of the Korean Environmental Sciences Society Conference
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• 2001.05a
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• pp.173-175
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• 2001

흡착에 필요한 최적의 세라믹 볼의 소성온도는 93$0^{\circ}C$가 가장 적당하다. 공업용수 중에 용존되어 있는 유기물 및 유해성분이 제거(COD나 $BOD_{5}$)가 가능하다. Fe와 Pb의 중 금속 제거의 경우 Pb의 경우가 제거 효율이 더 크며, 이에 따른 mechanism으로 이온교환이온이 Pb의 경우 2가 양이온이기에 더욱 효율이 크고 Fe의 경우는 수화하여 구조적인 붕괴를 일으키며, 2가와 3가의 공존하므로 Pb보다 제거율이 낮다. Fe와 Pb 중금속수를 1시간 동안 제거하여 Freundlich형 등온식에 따른 계산 결과 5,10ppm에서 1/n의 수치가 2 이상을 넘지 않고 있고, 500, 1000ppm의 경우는 등온이온교환으로 할 때 1/n의 수치가 2에 근접하므로 분말의 경우에 비해 제거율이 낮지는 않다. 그러므로 경제적 이점과 재활용면에서 볼의 사용이 우수하다는 것을 알 수 있다. 장치의 용기에 비례하여 볼 때 볼의 양은 600g이 가장 적당한 양이다. 등온교환의 경우 Apatite(HAp)를 이용한 분말의 제거율 보다 약간 낮으나 분말의 경우 사용 후 취급이 용이하지 않고 2차적 오염이 예상되므로 세라믹 볼의 경우 환경친화성재료로 여러 가지의 수처라 공정에 적용이 가능할 것으로 판단된다.