• Title/Summary/Keyword: Constant potential

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Magnetocrystalline Anisotropy of α''-Fe16N2 (α''-Fe16N2의 자기결정이방성)

  • Khan, Imran;Son, Jicheol;Hong, Jisang
    • Journal of the Korean Magnetics Society
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    • v.26 no.4
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    • pp.115-118
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    • 2016
  • We investigated the magnetocrystalline anisotropy of pure ${\alpha}^{{\prime}{\prime}}-Fe_{16}N_2$ by using full-potential linearized augmented plane wave method (FLAPW). A very high magnetic moment was obtained for Fe (4d) site due to the lattice expansion in the z-direction, while the magnetic moment of Fe (4e) and (8h) site were suppressed due to hybridization with neighboring N atom. The calculated spin magnetic moments for different Fe sites (4d, 4e and 8h) were in good agreement with previously reported values. Due to the tetragonal distortion, we found a very large uniaxial anisotropy constant of $0.58MJ/m^3$. Besides, a high value of magnetization of 1.76MA/m was obtained. In additon, the estimated coercive field and maximum energy product of 6.51 kOe and 71.7 MGOe were obtained for pure ${\alpha}^{{\prime}{\prime}}-Fe_{16}N_2$. This may suggest that the ${\alpha}^{{\prime}{\prime}}-Fe_{16}N_2$ can be utilized for potential rare-earth free permanent magnet material.

Electrochemical Behavior of UCl3 and GdCl3 in LiCl-KCl Molten Salt (LiCl-KCl 고온 용융염 내 UCl3 및 GdCl3의 전기화학적 거동 연구)

  • Min, Seul-Ki;Bae, Sang-Eun;Park, Yong-Joon;Song, Kyu-Seok
    • Journal of the Korean Electrochemical Society
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    • v.12 no.3
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    • pp.276-281
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    • 2009
  • Electrochemical behaviors of $U^{3+}$ and $Gd^{3+}$ were investigated in LiCl-KCl eutectic molten salt by using various electrochemical techniques. The electrodeposition and dissolution currents for uranium show the maximum at -1.51V and -1.35V, respectively while, for gadolinium,at -2.15V and -1.9V, respectively. In case of LiCl-KCl molten salt containing both of $U^{3+}$ and $Gd^{3+}$, the peak potential of electrodeposition of gadolinium shifts to more positive potential than in the solution without $U^{3+}$. The potentials in chronopotentiometric data suddenly dropped to negative value as soon as the reduction currents were applied and became constant at the potential around which the $U^{3+}$ and $Gd^{3+}$ are electrodeposited. The results of normal pulse voltammetry (NPV) and square wave voltammetry show that those methods can be used to qualitatively analyze the elements in the melts. Especially, the differentiation of NPV result was found to be useful for the separation of the peaks of which potentials are close each other.

Voltammetric Determination of Cu(II) Ion at a Chemically Modified Carbon-Paste Electrode Containing 1-(2-pyridylazo)-2-naphthol (1-(2-Pyridylazo)-2-naphthol 수식전극을 사용한 Cu(II) 이온의 전압전류법적 정량)

  • Jun-Ung Bae;Hee Sook Jun;Hye-Young Jang
    • Journal of the Korean Chemical Society
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    • v.37 no.8
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    • pp.723-729
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    • 1993
  • Cu(II) ion-responsive chemically modifed electrodes (CMEs) were constructed by incorporating 1-(2-pyridylazo)-2-naphthol (PAN) into a conventional carbon-paste mixture of graphite powder and Nujol oil. Cu(II) ion was chemically deposited on the surface of the PAN-chemically modified electrode in the absence of an applied potential by immersion of the electrode in a buffer solution (pH 3.2) containing Cu(II) ion, and then reduced at a constant potential in 0.1 M KNO$_3$. And a well-defined voltammetric peak could be obtained by scanning the potential to the positive direction. The electrode surface could be regenerated with exposure to acid solution and reused for the determination of Cu(II) ion. In 5 deposition / measurement / regeneration cycles, the response could be reproduced with 6.1${\%}$ relative standard deviation. In case of using the differential pulse voltammetry, the calibration curve for Cu(II) was linear over the range of 2.0 ${times}$ 10$^{-7}$ ∼ 1.0 ${times}$ 10$^{-6}$ M. And the detection limit was 6.0 ${times}$ 10$^{-8}$ M. Studies of the effect of diverse ions showed that Co, Ni, Zn, Pb, Mg and Ag ions added 10 times more than Cu(II) ion did not influence on the determination of Cu(II) ion, except EDTA and oxalate ions.

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Magnetic Properties of Cr Substituted SiTe Compounds (SiTe에 Cr을 치환한 화합물의 자기적 성질)

  • Landge, Kalpana;Bialek, Beata;Lee, Jae-Il
    • Journal of the Korean Magnetics Society
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    • v.21 no.4
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    • pp.127-131
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    • 2011
  • In this paper, we study the electronic and magnetic properties of Cr substituted SiTe in the rock-salt structure compound using the full potential linearized augmented plane wave method within the generalized gradient approximation to the exchange correlation potential. Two stoichiometries are studied: $CrSi_3Te_4$ with 25 %, and $CrSiTe_2$ with 50 % Cr substitution. We found, from the total energy calculations, that the equilibrium lattice constant for cubic $CrSi_3Te_4$ is 11.64 a.u. and a = 7.89 a.u. and c = 11.13 a.u. for tetragonal $CrSiTe_2$. The integer value of the calculated magnetic moment per unit cell, $4{\mu}_B$ for $CrSiTe_2$ suggests that this compound is halfmetallic. The magnetic moment per unit cell for $CrSi_3Te_4$ is slightly larger than $4{\mu}_B$. The magnetic moment on Cr atoms are 3.61 and $3.62{\mu}_B$ in the $CrSi_3Te_4$ and $CrSiTe_2$, respectively. The presence of Cr atoms causes that the other atoms become slightly magnetized in both compounds. The electronic properties and the magnetism are discussed with the calculated spin-polarized density of states.

Application of Rare Earth Compounds for the Treatment of Phosphate and Fluoride in Wastewater (인산염 및 불소폐수 처리제로서의 희토류 화합물 적용에 관한 연구)

  • Kim, Jin-Wha;Shin, Sung-Hye;Song, Hye-Won;Kim, Dong-Su;Woo, Sang-Mo;Kwon, Young-Shik
    • Journal of Korean Society of Environmental Engineers
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    • v.22 no.6
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    • pp.1127-1137
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    • 2000
  • Applications of lanthanum ion and crude rare earth chloride to the phosphate wastewater and fluorine wastewater, respectively, as treatment agents were studied. For the investigation of phosphate removal characteristics according to the amount of lanthanum ion, initial phosphate content was decreased by about 50% when molar ratio of [$La^{3+}$]:[$PO_4{^{3-}}-P$] was 0.25 and nearly all of phosphate was removed when the molar ratio of [$La^{3+}$]:[$PO_4{^{3-}}-P$] to be doubled. The removal of phosphate by $La^{3+}$ appeared to reach equilibrium state rapidly, and it was exothermic reaction since the removed amount of phosphate was diminished somewhat when the reaction temperature was increased. The zeta potential of combined particulate compound of lanthanum ion and phosphate was located for its isoelectric point at pH 5.5 and the turbidity of treated wastewater was found to vary according to the pH in a similar manner as the absolute value of zeta potential of the combined particulate compound did. For the treatment of fluorine wastewater by crude rare earth chloride, the remaining fluorine content after treatment decreased as the dosage of crude rare earth chloride increased. Whereas, the turbidity of treated wastewater and the amount of sludge generated were shown to increase as more crude rare earth chloride was added. The remaining fluorine content and the turbidity of treated wastewater were decreased and the amount of sludge generated was observed to increase according the increase of coagulant dosage under the condition of constant input of crude rare earth chloride.

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Influence of Grass Cover on Water Use and Shoot Growth of Young 'Fuji'/M.26 Apple Trees at Three Soil Water Regimes in Double Pot Lysimeters (토양수분영역을 달리한 double pot-lysimeter에서 자라는 '후지'/M.26 사과나무의 수분이용과 신초 생장에 미치는 잔디피복의 영향)

  • Ro, Hee-Myong
    • Korean Journal of Soil Science and Fertilizer
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    • v.32 no.4
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    • pp.357-364
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    • 1999
  • This study measures the influence of grass cover on water use and shoot growth of apple trees growing under different soil water regimes in temperate climate conditions and evaluates monthly crop coefficients of such conditions during four months of the growing season in 1995. To do so, double pot lysimeter experiments of 3-year-old Fuji' apple (Males domestica Borkh.) trees under a transparent rain shield were designed and installed. Trees were triplicate under three soil water regimes: (A) drip-irrigation at -50 kPa of soil matric potential (IR50). (B) drip-irrigation at -80 kPa of soil matric potential (IR80), and (C) constant shallow water table at 0.45 m below the soil surface (WT45). In each treatment, two soil surface conditions were tested: the soil surface bare, and covered with turf grasses. Mean monthly water use increased with increasing soil matric potential for drip irrigation and was greatest in the WT45 treatment. Monthly crop coefficients increased linearly in time for drip-irrigated apple trees ($r^2$ values of $0.953^{***}$ for turf grass-covered system and of $0.862^{***}$ for bare surface system), while those obtained in the WT45 treatment fluctuated, Duncan's multiple range tests for shoot growth showed that grass-covered IR50 was most favorable to apple trees. while bare surface waterlogged situation was most adverse at least in part due to a lack of oxygen in the root zone. Mid-season leaf Kjeldahl-N was higher in drip-irrigated apple trees than in WT45 trees, while soil Kjeldahl-N was not different irrespective of treatments.

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Reactivities of Di-iso-butylnitrosoamine by Anodic Film Formed on Metals (산화피막전극을 이용한 디이소부틸니트로소아민의 전극반응)

  • Hwang Kum-Sho
    • Korean Journal of Fisheries and Aquatic Sciences
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    • v.14 no.2
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    • pp.94-102
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    • 1981
  • To investigate the characteristics of anodic film formed on metals and the reactivities of organic inhibitor Di-iso-butylnitrosoamine (DBNA) in sea water. the cathodic reactions of anodic film formed on metals were carried out by using the potential drop method and galvanostatic method at $25^{\circ}C$. The investigated results are as follows: The anodic films formed on aluminum and zinc in 60mM $DBNA+9\%_{\circ}$ sea water did not show-changes of potential drop. However, those formed on lead and copper were reasonable electrodes. It was concluded that cathodic reactivities of proton through the anodic film in aqueous solution were constant without regard to the kinds of metals used with anodic film electrode at operated current density ranges, because the values of transition time obtained in 0.5M sodium chloride solution and $9\%_{\circ}$ sea water nearly coincided. The values of transition time of the first step by the galvanostatic method were obtained from 0.22 to 1.40 sec ranges far less than one minute. Therefore, it suggested that cathodic reactions of proton through the anodic film were mainly controlled by diffusion/adsorption process. The differences of between $\tau_{1}/4$ in $9\%_{\circ}$ sea water and $\tau_{1}/4$ in 60mM $DBNA+9\%_{\circ}$ sea water, and between $E_{1}/4$ in sea water and $E_{1}/4$ in 60mM $DBNA+9\%_{\circ}$ sea water at the constant current density with $1.9\times10^{-4}\sim5.0{\times}10^{-6}\;amp/cm^2$ were 0.06 sec and 0.53 v. respectively and cathodic reactions of DBNA on the anodic film electrodes were chiefly controlled by adsorption/diffusion process. The reason that adsorption quantities of proton on anodic film formed on aluminum and zinc in aqueous solutions were much more than those on lead and copper, seems to lie due mostly to the number of porosity produced on anodic film used.

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Estimation of Nitrogen Mineralization of Organic Amendments Affected by Nitrogen Content in Upland Soil Conditions (밭토양 조건에서 질소함량별 유기자원의 질소 무기화율 추정)

  • Lim, Jin-Soo;Lee, Bang-Hyun;Kang, Seung-Hee
    • Korean Journal of Environmental Agriculture
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    • v.38 no.4
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    • pp.262-268
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    • 2019
  • BACKGROUND: To investigate mineralization characteristics of organic resources in the soil, five materials (rice straw, cow manure sawdust compost, microorganism compost, mixed oil-cake, and amino acid fertilizer) were treated according to the nitrogen content, and an indoor incubation experiment was conducted for 128 days. The results of this analysis were applied to determine the nitrogen mineralization pattern of these organic resources. METHODS AND RESULTS: During the constant temperature incubation period, the nitrogen net mineralization rate of the organic resources was the highest in the amino acid fertilizer with the highest nitrogen content, and the lowest in the rice straw with the lowest nitrogen content. A positive correlation (0.96) was observed between the potential nitrogen mineralization rate and total nitrogen content. The mineralization rate constant, k, was negatively correlated with the organic matter (-0.96) and carbon content (-0.97). The nitrogen mineralization rate during the first cropping season, as estimated by the model, was 6.6%, 11.6%, 30.9%, 70.7%, and 81.0% for the rice straw, the cow manure sawdust compost, the microorganism compost, the mixed oil-cake, and the amino acid fertilizer, respectively. CONCLUSION: The nitrogen mineralization rate varies depending on the type of organic resources or the nitrogen content; thus, it can be used as an index for determining the nitrogen supply characteristics of the organic resource. Organic resources such as compost with low nitrogen content or those undergoing fermentation contain organic nitrogen. Organic nitrogen is stabilized during the composting process. Therefore, as the nitrogen mineralization rate of these resources is lower than that of non-fermented organic resources, it is desirable to use the fermented organic materials only to improve soil physical properties rather than to supply nutrients for the required amount of fertilizer.

Effect of Electrochemical Reduction of Ruthenium Black Cathode Catalyst on the Performance of Polymer Electrolyte Membrane Fuel Cells (캐소드 루테늄 촉매의 전기화학적 환원 처리가 고분자 전해질 연료전지 성능에 미치는 영향)

  • Choi, Jong-Ho
    • Journal of the Korean Electrochemical Society
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    • v.14 no.2
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    • pp.110-116
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    • 2011
  • Ru black was used for cathode catalyst in polymer electrolyte membrane fuel cell which showed low performance at the initial test. However, it was observed that the performance of Ru black cathode was dramatically enhanced after certain kind of experiment compared with initial one. It might be due to an electrochemical treatment in which a voltage was applied to the Ru cathode for constant period time. When a constant potential of 0.1 V was applied to Ru cathode for 30 min, the fuel cell performance of Ru cathode showed the best results. In order to investigate the effect of electrochemical treatment on the performance enhancement, the characteristics of electrochemically treated Ru black was compared with that of Ru black which was reduced under $H_2$ atmosphere. From XRD results, it was turned out that Ru black was not completely converted to metallic Ru by electrochemical treatment, but it is sufficient to be one of reasons for the performance enhancement. According to the results of CO stripping voltammetry, it was observed that some Ru was removed from Ru electrode by electrochemical treatment which might have a bad effect on the fuel cell performance. The removal of some Ru from as-received Ru black by electrochemical treatment is also another reason for the enhancement of fuel cell performance.

Adsorption and residues of EPN in the soil of Cheju Island (제주도 토양에서 EPN의 용탈과 잔류)

  • Kim, Jung-Ho;Kam, Sang-Kyu
    • The Korean Journal of Pesticide Science
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    • v.4 no.1
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    • pp.19-25
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    • 2000
  • The adsorption and leaching of organophosphorus pesticide, EPN (O-ethyl-O-4 -nitrophenyl phenyl phosphonothioate) were investigated in Namwon soil(black volcanic soil), Aewol soil(very dark brown volcanic soil) and Mureung soil(dark brown nonvolcanic soil) in Cheju Island. The residue of EPN was surveyed on coastal environment of Cheju in Aug. 1996. The organic matter of Namwon soil, Aewol soil and Mureung soil was 19.8, 6.2 and 2.4%, respectively. The cation exchange capacity of Namwon soil, Aewol soil and Mureung soil was 24.8, 13.0 and 9.5 meq/100 g, respectively. The Freundlich constant, k value, was 89.4, 26.9 and 9.25 for Namwon soil, Aewol soil and Mureung soil, respectively. The k value of Namwon soil with very high organic matter content and cation exchange capacity was the highest for Aewol soil and Mureung soil. The Freundlich constant, 1/n, show a high correlation with organic matter content, i.e. it is less than unity for organic matter rich soil of Namwon soil and greater than unity for organic matter poor soil of Mureung soil. The leaching of EPN was slower for Namwon soil with high k values, and faster for Mureung soil with low k values. The results of the study was demonstrated the potential of pollution for EPN have little leached into soil environment. EPN was not detected in seawater and sediment in the coastal environment in Cheju Island. EPN used in the farm on tile Cheju island were not residued in the coastal environment.

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