• Title/Summary/Keyword: dissolved metal

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Preparation of $Mn_{0.5}Zn_{0.5}$ Ferrite Powder by Coprecipition Process (공침법에 의한 $Mn_{0.5}Zn_{0.5}$ Ferrite 분말제조연구)

  • 엄태형;서동수
    • Proceedings of the Korean Institute of Electrical and Electronic Material Engineers Conference
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    • 1991.10a
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    • pp.33-36
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    • 1991
  • For its outstanding magnetic property, preparations of MnZn ferrite were studied with various method. In this study, MnZn ferrite powders were prepared from ammonium oxalate and mixed metal sulfate by the controlled coprecipitation process. Considering to low dissolved each metal ion, high production yield and particle size, the established optimum reaction conditon by the statistical analysis of each results are that reaction temperature is $25^{\circ}C$, concentration of metal sulfate is 0.3M, molar ratio of ammonium oxalate/metal sulfate is 1.1:1. The effective experimental factor and characterization of the precipitated powder at optimum condition were studied.

WITNESSING DISSOLUTION OF A STAR CLUSTER IN THE SEXTANS DWARF GALAXY

  • Kim, Hak-Sub;Han, Sang-Il;Joo, Seok-Joo;Yoon, Suk-Jin
    • The Bulletin of The Korean Astronomical Society
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    • v.43 no.1
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    • pp.32.3-32.3
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    • 2018
  • We report a possible discovery of a relic of a dissolved star cluster in the Sextans dwarf spheroidal galaxy. Using the hk index (${\equiv}$(Ca-b)-(b-y)) as a photometric metallicity indicator, we have successfully discriminated the metal-poor and metal-rich stars in the galaxy and found an unexpected number density peak of metal-poor stars near the galaxy center. The analysis of color-magnitude diagrams reveals that they appear to be originated from an old, metal-poor globular cluster which might be slightly farther than the bulk of field stars in the galaxy. This supports the presence of the star cluster remnants in the galaxy which have been suggested by previous studies. If confirmed, dissolution of a star cluster provides a piece of evidence of a cored dark-matter halo profile for the Sextans dwarf galaxy.

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ADSORPTION OF PB(2) ON METAL OXIDE PARTICLES CONTAINING ALUMINUM AND TITANIUM IN AQUEOUS SOLUTIONS

  • Kim, Moon-Sun;Hong, Sung-Chul;Chung, JayGwanG.
    • Environmental Engineering Research
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    • v.10 no.2
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    • pp.45-53
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    • 2005
  • Metal oxide particles with mole ratio of aluminum: titanium of 1:1 were synthesized by a sol-gel method. Langmuir (a) and Freundlich (b) adsorption isotherms of dissolved lead [Pb(Ⅱ)] ion on the metal oxide particles containing aluminum and titanium were determined as follows, respectively,(a) , (b) at pH 6where, correlation coefficients (R2) of Langmuir and Freundlich adsorption isotherms were 0.95 and 0.96, respectively.The overall adsorption rate of Pb(Ⅱ) on the metal oxide particles containing aluminum and titanium was determined by a differential bed reactor. The overall adsorption rate at pH 6 was as a following equation.at pH 6

Assessment Techniques of Heavy Metal Bioavailability in Soil - A critical Review (토양 중 중금속 생물유효도 평가방법 - 총설)

  • Kim, Kwon-Rae;Owens, Gary;Naidu, Ravi;Kim, Kye-Hoon
    • Korean Journal of Soil Science and Fertilizer
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    • v.40 no.4
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    • pp.311-325
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    • 2007
  • The concept of metal bioavailability, rather than total metal in soils, is increasingly becoming important for a thorough understanding of risk assessment and remediation. This is because bioavailable metals generally represented by the labile or soluble metal components existing as either free ions or soluble complexed ions are likely to be accessible to receptor organismsrather than heavy metals tightly bound on soil surface. Consequently, many researchers have investigated the bioavailability of metals in both soil and solution phases together with the key soil properties influencing bioavailability. In order to study bioavailability changes various techniques have been developed including chemical based extraction (weak salt solution extraction, chelate extraction, etc.) and speciation of metals using devices such as ion selective electrode (ISE) and diffusive gradient in the thin film (DGT). Changes in soil metal bioavailability typically occur through adsorption/desorption reactions of metal ions exchanged between soil solution and soil binding sites in response to changes in environment factors such as soil pH, organic matter (OM), dissolved organic carbon (DOC), low-molecular weight organic acids (LMWOAs), and index cations. Increasesin soil pH result in decreases in metal bioavailability through adsorption of metal ions on deprotonated binding sites. Organic matter may also decrease metal bioavailability by providing more negatively charged binding sites, and metal bioavailability can also be decreases as concentrations of DOC and LMWOAs increase as these both form strong chelate complexeswith metal ions in soil solution. The interaction of metal ions with these soil properties also varies depending on the soil and metal type.

Geochemical Reaction Processes and Controls on the Coal Mine Drainage using Pilot-scale Inclined Clarifiers (Pilot 규모의 경사판 침전지 시험을 통한 국내 석탄광산배수내 부유물질의 지구화학적 반응특성 및 조정영향)

  • Lee, SangHoon;Oh, Minah;Lee, Jai-Young;Kwon, Eunhye;Kim, Doyoung;Kim, DukMin
    • Journal of Soil and Groundwater Environment
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    • v.18 no.7
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    • pp.73-80
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    • 2013
  • Fine suspended solids from coal mine drainage were treated in the treating plant, using two different pilot-scale inclined clarifiers: radial and lamella types. Suspended solids in the mine drainage were monitored along with other geochemical factors, and metal contents. Fe and Mn are the main chemical components in the drainage, which exist predominantly as total metal forms, whereas dissolved portion is negligible. The raw mine drainage is subject to physical and chemical treatment using $CaCO_3$ and NaOH, therefore the suspended solids are thought to be composed of Fe and Mn precipitates, possibly $Fe(OH)_3$, along with carbonate precipitates. The elemental composition of precipitates are confirmed by SEM-EDS analysis. As nearly all the dissolved ions were precipitated in the primary process by $CaCO_3$, no further aeration or prolonged oxygenation are of necessity in this plant. Adoption of inclined clarifier proved to be effective in treating fine suspended solids in the current plant. Successful application of the inclined clarifier will also be beneficial to improve the current treating process by excluding the current application of chemical agent in the first stage. The final effluents from the pilot plant meet the national standards and the low dissolved Fe and Mn contents are expected not to cause secondary precipitation after discharge.

Removal of Dissolved Heavy Metals in Abandoned Mine Drainage by Ozone Oxidation System (오존산화를 이용한 폐광산배수 내 용존 중금속 제거에 관한 연구)

  • Seo, Suk Ho;Ahn, Kwang Ho;Lee, Jung Kyu;Kim, Gun Jooung;Chu, Kyoung Hoon;Ra, Young Hyun;Ko, Kwang Baik
    • Journal of Korean Society on Water Environment
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    • v.26 no.5
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    • pp.725-731
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    • 2010
  • This study was to evaluate the ozone oxidation of dissolved Fe, Mn, $SO{_4}^{2-}$ ions and color in abandoned mining drainage by conducting a bench-scale operation at various reaction times in an ozone reactor. The influent was collected from an abandoned mine drainage (AMD) near the J Mine in Jungsungun, Kangwon Province. The ozone reactor was operated at ozone reaction times of 10, 20 and 30 min with ozone doses of 0.0 and $2.4g\;O_3/hr$. Samples from each effluent from subsequent sand filtration were regularly collected and analyzed for pH, Fe, Mn, Al, Cr, Hg, $SO{_4}^{2-}$, alkalinity, color, ORP, TDS and EC. The effluent concentrations of Fe and Mn from the sand filter were less than 0.1 mg/L, which were below the concentrations on Korean drinking water quality standards (Fe, Mn < 0.30 mg/L). The influent $SO{_4}^{2-}$, concentrations were not noticeably changed during this ozone oxidation. Cr and Hg in the raw wastewater from the abandoned mining drainage were not detected in this study. The experimental result shows that the ozone oxidation of dissolved heavy metals and subsequent sand filtration of metal precipitates are desirable alternative for removing heavy metals in AMD.

Fabrication and Characteristics of Pd/Pt Gate MISFET Sensor for Dissolved Hydrogen in Oil (유중 용존수소 감지를 위한 Pd/Pt Gate MISFET 센서의 제조와 그 특성)

  • Baek, Tae-Sung;Lee, Jae-Gon;Choin, Sie-Young
    • Journal of Sensor Science and Technology
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    • v.5 no.4
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    • pp.41-46
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    • 1996
  • The Pd/Pt gate MISFET type hydrogen sensors, for detecting dissolved hydrogen gas in the transformer oil, were fabricated and their characteristics were investigated. These sensors including diffused resister heater and temperature monitoring diode were fabricated on the same chip by a conventional silicon process technique. The differential pair plays a role in minimizing the intrinsic voltage drift of the MISFET. To avoid the drift of the sensors induced by the hydrogen, the gate insulators of both FETs were constructed with double layers of silicon dioxide and silicon nitride. In order to eliminate the blister formation on the surface of the hydrogen sensing gate metal, Pt and Pd double metal layers were deposited on the gate insulator. The hydrogen response of the Pd/Pt gate MISFET suggests that the proposed sensor can detect the dissolved hydrogen in transformer oil with 40mV/10ppm of sensitivity and 0.14mV/day of stability.

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Distribution of Dissolved Heavy Metals Released during Stabilizing Processes of Soft Sea-Bottom using Cement Stabilizers (시멘트 고화제 고결공법에 따른 공사장 주변해수의 용존성 중금속 농도 변화)

  • Kim, Kyung-Tae;Kim, Eun-Soo;Oh, Young-Min;Chung, Kyung-Ho;Cho, Sung-Rok;Park, Jun-Kun
    • Journal of the Korean Society for Marine Environment & Energy
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    • v.8 no.2
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    • pp.74-77
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    • 2005
  • The injection of cement stabilizer is used as one of ways to stabilize soft sea-bottom. However, this method makes an argument for the possibility of releasing heavy metals from the cement stabilizer to the seawater. To investigate the effect of the cement stabilizer on the seawater, field measurements were carried out in Ocheon harbor of the Chunsoo Bay. Although the highest concentrations of dissolved heavy metals were found in the surface seawater of the injection point and the metal concentrations decreased with distances, the levels of heavy metals in all the seawater met the demand of environmental criteria of Korea, US and UK.

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Treatment of Black Dross with Water and NaOH Solution (물과 수산화나트륨용액에 의한 블랙 드로스의 처리)

  • Xing, Wei Dong;Ahn, Byung Doo;Lee, Man Seung
    • Resources Recycling
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    • v.26 no.3
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    • pp.53-60
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    • 2017
  • Black dross contains metallic aluminium, alumina, silica, MgO, soluble salts together with minor ingredients. Control of silica in black dross is important in transforming the black dross into usable materials. First, most of the soluble salts (KCl and NaCl) in black dross were dissolved in water at reaction temperature of $50^{\circ}C$. Leaching behavior of silica, alumina, MgO and $TiO_2$ from the residue after water treatment was investigated by varying NaOH concentration and reaction temperature. Reaction temperature ($25{\sim}95^{\circ}C$) was favorable to the leaching of alumina but an optimum temperature existed for silica. MgO was not dissolved at all in the NaOH concentration range from 2 to 6 M. At the leaching condition of 5 M NaOH and reaction temperature of $95^{\circ}C$, approximately 80% of alumina and 68% of silica was dissolved.

Reduction of perchlorate using zero-valent titanium (ZVT) anode: reaction mechanism

  • Lee, Chunwoo;Batchelor, Bill;Park, Sung Hyuk;Han, Dong Suk;Abdel-Wahab, Ahmed;Kramer, Timothy A.
    • Advances in environmental research
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    • v.1 no.1
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    • pp.37-55
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    • 2012
  • Here we show that perchlorate reduction during pitting corrosion of zero-valent titanium (ZVT) is likely caused by dissolved titanium species, especially Ti(II). Several possible mechanisms were suggested based on the literature and were evaluated based on experimental observations. Direct reduction of perchlorate on the bare metal of the ZVT electrode was thermodynamically infeasible due to the high anodic potential that was applied. Other potential mechanisms were considered such as reduction by small ZVT metal particles released from the electrode and direct reduction on the oxide layer of the electrode where potential was sufficiently reduced by a high ohmic potential drop. However, these mechanisms were not supported by experimental results. The most likely mechanism for perchlorate reduction was that during pitting corrosion, in which ZVT is partially oxidized to form dissolved ions such as Ti(II), which diffuse from the electrode surface and react with perchlorate in solution. This mechanism is supported by measurements of the dissolution valence and the molar ratio of ZVT consumed to perchlorate reduced (${\Delta}Ti(0)/{\Delta}ClO_4{^-}$). The results shown in this study demonstrate that ZVT undergoing pitting corrosion has the capability to chemically reduce perchlorate by producing dissolved Ti(II) and therefore, it has the potential to be applied in treatment systems. On the other hand, the results of this research imply that the application of ZVT undergoing pitting corrosion in treatment systems may not be feasible now due to several factors, including material and electricity costs and possible chloride oxidation.