• Title/Summary/Keyword: Separation of Fe and P

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A $PbTiO_{3}$ Transmitting/P(VDF-TrFE) Receiving Wideband Ultrasonic Transducer in VHF Band (VHF 대역에 있어서 $PbTiO_{3}$송신/P(VDF-TrFE) 수신 광대역 초음파변환자)

  • Ha, Kang-Lyeol;Kim, Moo-Joon;Kim, Jung-Ho;Kim, Jung-Soon
    • The Journal of the Acoustical Society of Korea
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    • v.23 no.4E
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    • pp.120-124
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    • 2004
  • A new type of high frequency wideband ultrasonic transducer with a separation between a transmitter and a receiver was proposed and its characteristics were simulated using a PSpice model. The piezoelectric ceramic $PbTiO_{3}$ as a transmitter and the piezoelectric copolymer P(VDF- TrFE) as a receiver were used for high sensitivity and wide bandwidth, respectively. The characteristics of the focusing transducer with center frequency of approximately 35MHz fabricated in this study showed very wide bandwidth, which could give an axial spatial resolution better than $30{\mu}m$ in B-mode image for biological tissues.

Effect of Spinodal Phase Separation and Phase Dissolution on a Succeeding Crystallization in P(VDF/TrFE)/PBA Blends (P(VDF/TrFE)/PBA 블렌드의 스피노달 상분리 및 상용해가 결정화거동에 미치는 영향)

  • 김갑진;이종순
    • Proceedings of the Korean Fiber Society Conference
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    • 2002.04a
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    • pp.207-210
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    • 2002
  • PVDF는 측쇄에 C=O기를 갖는 고분자인 PMMA와 PVAc와의 블렌드 및 주쇄에 C=O기를 갖는 poly(1,4-butylene adipate) (PBA)와의 블렌드에서 PVDF의 융점보다 상당히 높은 온도에서 LCST거동을 보이고 있음이 알려져 있다. 그런데 PVDF/PMMA와 PVDF/PVAC 블렌드계에서는 LCST가 고분자의 열분해온도와 유사하여 LCST거동을 실험적으로 관찰하기 어려웠다. 그런데 PVDF/PBA 블렌드계에서는 실험적으로 측정할 수 있을 정도로 LCST가 낮아지긴 하였지만 PBA의 열분해를 완전히 배제하기엔 아직도 높은 온도이다.[1] (중략)

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Enhancement of phosphate removal using stabilized Fe-Mn particle (Fe-Mn 입자의 안정화를 통한 인산염 효율 향상)

  • Seoyeon Kang;Jeongwoo Shin;Byugnryul An
    • Journal of Korean Society of Water and Wastewater
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    • v.37 no.6
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    • pp.375-382
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    • 2023
  • The binary oxide adsorbent using Fe and Mn (Fe-Mn) has been prepared by precipitation method to enhance the removal of phosphate. Different amounts of chitosan, a natural organic polymer, were used during preparation of Fe-Mn as a stabilizer to protect an aggregation of Fe-Mn particles. The optimal amount of chitosan has been determined considering the separation of the Fe-Mn particles by gravity from solution and highest removal efficiency of phosphate (Fe-Mn10). The application of Fe-Mn10 increased removal efficiency at least 15% compared to bare Fe-Mn. According to the Langmuir isotherm model, the maximum uptake (qm) and affinity coefficient (b) were calculated to be 184 and 240 mg/g, and 4.28 and 7.30 L/mg for Fe-Mn and Fe-Mn10, respectively, indicating 30% and 70% increase. The effect of pH showed that the removal efficiency of phosphate was decrease with increase of pH regardless of type of adsorbent. The enhanced removal efficiency for Fe-Mn10 was maintained in entire range of pH. In the kinetics, both adsorbents obtained 70% removal efficiency within 5 min and 90% removal efficiency was achieved at 1 h. Pseudo second order (PSO) kinetic model showed higher correlation of determination (R2), suggesting chemisorption was the primary phosphate adsorption for both Fe-Mn and Fe-Mn10.

Development of the Purification Method of Ovotransferrin in Egg White (난백 내 Ovotransferrin의 분리방법에 관한 연구)

  • Jang, A.;Jo, Y.J.;Lee, M.;Kim, J.C.
    • Journal of Animal Science and Technology
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    • v.47 no.6
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    • pp.1025-1032
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    • 2005
  • This study was carried out to separate ovotransferrin in chicken egg white by gel chromatography and heparin affinity chromatography. In gel filtration which was performed with 50mM Phosphate buffer (pH 7.2, 0.15M salt) at a flow rate of 2.0 ml/min, ovotransferrin and ovalbumin were eluted together in fraction number 11-16. In order to separate pure ovotransferrin, fraction No. 12-14 of them which have high concentration of ovotransferrin were concentrated and rechromatographed. However, the ovotransferrin did not separated clearly. In heparin affinity chromatography, the separation was performed with 50mM ethylaminetetraacetic acid (EDTA, pH7.2) and 50mM Phosphate buffer (pH 7.2, 0.15M salt contained) on ferrous and ferric ion saturated column at as same flow rate as gel filtration system's. Ovotransferrin and albumin were eluted together at 10-15min (fraction No.3) and 15-20min (fraction No.4), respectively. However, purified ovotransferrin was eluted at 156-165min and 165-175min (tube No.32-33) with 50 mM phosphate buffer (pH 7.2, 0.15M salt free), respectively. Heparin affinity chromatography with ferric ion saturated column was resulted in the best separation of ovotransferrin rather than separation by gel chromatography and ferrous ion saturated heparin affinity chromatography.

Preparation of Carrier-free Fe-59 by Korean TRIGA Mark Ⅱ Reactor (無擔體 鐵-59製造에 關한 硏究)

  • Park, Keung-Shik
    • Journal of the Korean Chemical Society
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    • v.9 no.2
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    • pp.96-100
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    • 1965
  • Possibility on carrier-free Fe-59 preparation by Korean TRIGA Mark Ⅱ reactor was investigated, namely average cross section on $Co^{59}$(n,p) $Fe^{59}$ reaction, separation by anion exchange resin and radiochemical purity. Radiochemical purity of Fe-59 separated was checked by the method of ${\gamma}$-ray spectrometry with 256-multichannel pulse height analyzer and of half life determination. This method permits Fe-59 preparation with radiochemical purity of > 99.9%.

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Quantitative Separation of Some Transition Metals by Cation Exchange Chromatography (陽이온 交換크로마토그라피에 의한 轉移元素의 分離)

  • Kim, Tong-Yup;Cha, Ki-Won;Park, Kee-Chae
    • Journal of the Korean Chemical Society
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    • v.8 no.2
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    • pp.62-64
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    • 1964
  • The cation exchange chromatographic studies for the analysis of transition metals have been described. The quantitative separation of a mixture of Fe(Ⅲ), Cu(II), Zn(II), Ni(II), Cd(II), Co(II) and Mn(II) has been obtained by elution, through a 28cm column of the resin, Dowex 50 ${\times}$ 4 (100∼200 mesh), using 0.45 M $NaNO_3$+0.05 M Na-tartrate solution as eluent, starting with the eluent of pH 3.5, followed stepwise by pH 4.0 and 4.5. A comparison between the calculated and the observed peak positions in the elution curve has been shown. The relative stability constants for tartrate complexes of some transition metals have been calculated by using distribution ratios obtained in this separation procedure.

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Removal of Cobalt Ion by adsorbing Colloidal Flotation (흡착 교질 포말부선법에 의한 Cobalt Ion의 제거)

  • 정인하;이정원
    • Resources Recycling
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    • v.7 no.3
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    • pp.3-10
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    • 1998
  • Simulated waste liquid containing 50 ppm cobalt ion was treated by adsorbing colloidal flotation using Fe(III) or Al(IlI) as flocclant and a sodium lamyl sulfate as a collector. Parameters such as pH, surfactant concentration, Fe(III) or Al(III) concentration, gas flow rate, etc., W앙e considered. The flotation with Fe(III) showed 99.8% removal efficiency of cohalt on the conditions of initial cobalt ion concentration 50 ppm, pH 9.5, gas flow rate 70 ml/min, and flotation time 30 min. When the waste solution, was treated with 35% $H_2O_2$ prior to adsorbing colloidal flotation, the optimal pH for removing cobalt shifted m to weak alkaline range and flotation could be applied in wider range of pH as compared to non-use of $H_2O_2$. Additional use of 20 ppm Al(III) after precipitation of 50 ppm Co(II) with 50 ppm Fe(III) made the optimal pH range for preferable flotation w wider. Foreign ions such as, $NO_3^-$, $SO_4^{2-}$, $Na^+$, $Ca^{2+}$ were adopted and their effects were observed. Of which sulfate ion was f found to be detrimental to removal of cob퍼t ion by flotation. Coprecipitation of Co ion with Fe(III) and Al(III) resulted in b better removal efficiency of cobalt IOn 피 the presence of sulfate ion.

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Reversed-Phase Liquid Chromatographic Separation of Metal Ions by Chelate Formation with 1-(2-Pyridylazo)-2-Naphthol (역상 액체크로마토그래피에 의한 1-(2-Pyridylazo)-2-Naphthol과 킬레이트를 형성하는 금속이온의 분리)

  • Kang, Sam Woo;Park, Sun Ja
    • Journal of the Korean Chemical Society
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    • v.42 no.2
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    • pp.197-202
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    • 1998
  • 1-(2-Pyridylazo)-2-Naphthol (PAN) has been widely used as a spectrophotometric reagent and metallochromic indicator for many metal ions. In this work, the chelate reagent of PAN was used as mobile phase additive for the separation of metal ions by reversed phase chromatography. Metal ions could be detected by monitoring the effluent at 570 nm with spectrophotometric detector. In order to investigate retention behaviors of the metal ions, the chromatograms and capacity factors were obtained as the variation of pH, ionic strength and composition of organic modifier in mobile phase. Under the obtained optimum conditions, the mixtures of Fe(III), Ni(II), Cu(II), Zn(II) and Co(II) could be separated successfully and the calibration curves under the recommended conditions showed an excellent linearity. The detection limits(S/N) were feasible at the nanogram level.

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The spectrophotometric determination of undecylenic acid using tris (1,10-phenanthroline) Fe(II) chelate (Tris(1,10-phenathroline) Fe(II) chelate에 의한 undecylenic acid의 흡광광도 정량법)

  • 강삼식;백남호
    • YAKHAK HOEJI
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    • v.16 no.4
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    • pp.180-185
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    • 1972
  • A new spectrophotometric method was established for the determination of undecylenic acid. The method is based on the solvent extraction into nitrobenzene of the ion pair formed between tris(1,10-phenanthroline)Fe(II) chelate and the anion of undecylenic acid. The maximum absorbance of the extract in the organic phase was at 518nm. A maximum extraction was obtained at pH 9-11, when excess of at least 50-fold(molar) of the phenanthroline-Fe(II) chelate to undecylenic acid was present. The color intensity of the extracted species remained constant at room temperature for the several hours after separation of the organic layer. A linear relationship was obtained over the tested range of 5-20${\gamma}$/ml of undecylenic acid. The effect of several other fungicids on this method was investigated. The method was applied to the determination of undecylenic acid in preparations and the results were in good agreement with those added amounts.

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Pre-leaching of Lithium and Individual Separation/Recovery of Phosphorus and Iron from Waste Lithium Iron Phosphate Cathode Materials (폐리튬인산철 양극재로부터 리튬의 선침출 및 인과 철의 개별적 분리 회수 연구)

  • Hee-Seon Kim;Boram Kim;Dae-Weon Kim
    • Clean Technology
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    • v.30 no.1
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    • pp.28-36
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    • 2024
  • As demand for electric vehicles increases, the market for lithium-ion batteries is also rapidly increasing. The battery life of lithium-ion batteries is limited, so waste lithium-ion batteries are inevitably generated. Accordingly, lithium was selectively preleached from waste lithium iron phosphate (LiFePO4, hereafter referred to as the LFP) cathode material powder among lithium ion batteries, and iron phosphate (FePO4) powder was recovered. The recovered iron phosphate powder was mixed with alkaline sodium carbonate (Na2CO3) powder and heat treated to confirm its crystalline phase. The heat treatment temperature was set as a variable, and then the leaching rate and powder characteristics of each ingredient were compared after water leaching using Di-water. In this study, lithium showed a leaching rate of approximately 100%, and in the case of powder heat-treated at 800 ℃, phosphorus was leached by approximately 99%, and the leaching residue was confirmed to be a single crystal phase of Fe2O3. Therefore, in this study, lithium, phosphorus, and iron components were individually separated and recovered from waste LFP powder.