• Title/Summary/Keyword: chemical elements

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Correlation between rare earth elements in the chemical interactions of HT9 cladding

  • Lee, Eun Byul;Lee, Byoung Oon;Shim, Woo-Yong;Kim, Jun Hwan
    • Nuclear Engineering and Technology
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    • v.50 no.6
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    • pp.915-922
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    • 2018
  • Metallic fuel has been considered for sodium-cooled fast reactors because it can maximize the uranium resources. It generates rare earth elements as fission products, where it is reported by aggravating the fuel-cladding chemical interaction at the operating temperature. Rare earth elements form a multicomponent alloy (Ce-Nd-Pr-La-Sm-etc.) during reactor operation, where it shows a higher reaction thickness than a single element. Experiments have been carried out by simplifying multicomponent alloys for mono or binary systems because complex alloys have difficulty in the analysis. In previous experiments, xCe-yNd was fabricated with two elements, Ce and Nd, which have a major effect on the fuel-cladding chemical interaction, and the thickness of the reaction layer reached maximum when the rare earth elements ratio was 1:1. The objective of this study is to evaluate the effect and relationship of rare earth elements on such synergistic behavior. Single and binary rare earth model alloys were prepared by selecting five rare earth elements (Ce, Nd, Pr, La, and Sm). In the single system, Nd and Pr behaviors were close to diffusion, and Ce showed a eutectic reaction. In the binary system, Ce and Sm further increased the reaction layer, and La showed a non-synergy effect.

Chemical Speciations of Elements in the Fe-Mn Crusts by Sequential Extraction (단계별 추출법을 이용한 망간각 구성 원소의 존재 형태)

  • Kim, Jong-Uk;Moon, Jai-Woon;Chi, Sang-Bum;Ko, Young-Tak;Lee, Hyun-Bok
    • Ocean and Polar Research
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    • v.26 no.2
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    • pp.231-243
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    • 2004
  • Sequential extraction was carried out on twenty two subsamples of three ferromanganese crusts from three seamounts (Lemkein, Lomilik, and Litakpooki) near the Marshall Islands in the western Pacific. The extraction was designed to fractionate Fe-Mn crust forming elements into low defined groups: (1) exchangeable and carbornate, (2) Mn-oxide, (3) Fe-oxyhyd.oxide, and (4) residual fraction. X-ray diffraction result shows that target material were well removed by each extraction step except for CFA in phosphatized crusts generation. According to chemical analysis of each leachate, most of elements in the Fe-Mn crusts are bound with two major phases. Mn, Ba, Co, Ni, Zn, (Fe, Sr, Cu, and V) are strongly bounded with Mn-oxide $({\delta}-MnO_2)$ phase, whereas Fe, Ti, Zr, Mo, Pb, Al, Cu,(V, P, and Zn) show chemical affinity with Fe-oxyhydroxide phase. This result indicates that significant amount of Al, Ti, and Zr can not be explained by detrital origin. Ca, Mg, K, and Sr mainly occur as exchangeable elements and/or carbonate phase. Outermost layer 1 and inner layer 2 which are both young crusts generations are similar in chemical speciations of elements. However, some of Fe-oxyhydroxide bounded elements (Pb, Y, Mo, Ba, Al, and V) in phosphatized innermost layer 3 are released during phosphatization and incorporated into phosphate (Pb, Y, Mo, and Ba) or Mn-oxide phase (Al and V). Our sequential extraction results reveal that chemical speciations of elements in the hydrogenetic crusts are more or less different from interelemental relationship calculated by statistical method based on bulk chemistry.

Two Method for Evaluation of the Dipole Moment Matrix Elements (쌍극자모멘트 행렬요소를 계산하는 두가지 방법)

  • Sangwoon Ahn
    • Journal of the Korean Chemical Society
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    • v.22 no.4
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    • pp.229-238
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    • 1978
  • Two methods for evaluation of the dipole moment matrix elements are developed, one using the expansion method for spherical harmonics and the other the transformation method of the dipole moment matrix elements into overlap integrals for Mulliken. The numerical values of the dipole moment matrix elements evaluated by two methods are in agreement with each other.

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Distribution of Zirconium Between Salt And Bismuth During A Separation From Rare Earth Elements By A Reductive Extraction

  • S. W. Kwon;Lee, B. J.;B. G. Ahn;Kim, E. H.;J. H. Yoo
    • Proceedings of the Korean Radioactive Waste Society Conference
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    • 2004.02a
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    • pp.165-169
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    • 2004
  • It was studied on the reductive extraction between the eutectic salt and Bi metal phases. The solutes were zirconium and the rare earth elements, where zirconium was used as the surrogate for the transuranic(TRU) elements. All the experiments were performed in a glove box filled with argon gas. Two types of experimental conditions were used -high and low initial solute concentrations in salt. Li-Bi alloy was used as a reducing agent to reduce the high chemical activity of Li. The reductive extraction characteristics were examined using ICP, XRD and EPMA analysis. Zirconium was successfully separated from the rare earth elements by the reductive extraction method. The LiF-NaF-KF system was favorable among the fluoride salt systems, whereas the LiCl-KCl system was favorable among the chloride salt systems. When the solute concentrations were high, intermetallic compounds were found near the salt-metal interface.

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The Chemical Composition of HD47536: A Planetary Host Halo Giant with Possible 𝛌 Bootis Features and Signs of Interstellar Matter Accretion

  • Yushchenko, Alexander;Doikov, Dmytry;Andrievsky, Sergei;Jeong, Yeuncheol;Yushchenko, Volodymyr;Rittipruk, Pakakaew;Kovtyukh, Valery;Demessinova, Aizat;Gopka, Vira;Raikov, Alexander;Jeong, Kyung Sook
    • Journal of Astronomy and Space Sciences
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    • v.39 no.4
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    • pp.169-180
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    • 2022
  • We investigated the chemical composition of the planetary host halo star HD47536 via high-resolution spectral observations recorded using a 1.5 meter Cerro Tololo Inter-American Observatory (CTIO) telescope (Chile). Furthermore, we determined the abundances of 38 chemical elements. Both light and heavy elements were overabundant compared to the iron group elements. The abundance pattern of HD47536 was similar to that of halo-type stars, with an enrichment of heavy elements. We analyzed the relationships between the relative abundances of chemical elements and their second ionization potentials and condensation temperatures. We demonstrated that the interplay of charge-exchange reactions owing to the accretion of interstellar matter and the gas-dust separation mechanism can influence the initial abundances and can be used to qualitatively explain the abundance patterns in the atmosphere of HD47536.

Performance of a Group Candle Filter in a Hot Bench Unit

  • Park, Joo-Hong;Park, Gyung-Won
    • Journal of Energy Engineering
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    • v.8 no.1
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    • pp.143-149
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    • 1999
  • The mounting technology of ceramic candle elements utilizing disk spring was tested in a hot bench unit. Seven SiC candle elements were fixed in three groups by 2, 2, and 3 elements per group. And its performance was investigated in a hot gas stream using oil burned-exhaust gas. The experimental results showed that this mounting method gave a good performance enough to be useful for the particulate removal in the integrated gasification combined cycle (IGCC). Some operational characteristics of the groupfilter were observed.

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Study on the Addition and the Transfer of Alloying Elements in FCAW (FCAW에 의한 합금 성분의 첨가와 이행에 관한 연구)

  • 김경중;박관호
    • Journal of Welding and Joining
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    • v.1 no.2
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    • pp.76-82
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    • 1983
  • The chemical composition of deposit metal by flux cored arc welding can be easily regulated though addition of deoxidizers and alloying elements in cored flux and fluxes of flux coored wire arc analogous to those of coated electrode. It is necessary to investigate the transfer and yield efficiency due to addition of necessary alloy elements in deposit metal. This report is made to intorduce an experimental equation from the relation between welding condition and extent of penetration, deposit metal and weld melt slag and to estimate transfer and yield efficiency of alloy components in fluxes through chemical analysis of deposit metal.

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SPECTROSCOPIC STUDY ON RED GIANTS IN GLOBULAR CLUSTERS (구상성단 거성들의 분광 연구)

  • LEE SANG-GAK
    • Publications of The Korean Astronomical Society
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    • v.15 no.spc1
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    • pp.15-30
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    • 2000
  • A large scatter of the chemical abundances among globular cluster red giants has been observed. Especially the chemical elements C, N, O, Na, Mg, and Al vary form star to star within globular clusters. Except for $\omega$ Cen and M22, most globular clusters could be considered to be monometallic of their iron peak elements within error ranges. The variations in light elements among globuar cluster giants appear much more pronounced than in field halo giants of comparable Fe-peak metallicity. It has been found that in general the nitrogen abundance is anticorrelated with both carbon and oxygen, while it is correlated with Na and AI. These intracluster abundance inhomogeneities can be interpreted either by mixing of nucleosythesized material from the deep stellar interior during the red giant branch phase of evolution or by inhomogeneities of primordially processed material, from which the stars were formed. The simple way of distingushing between two senarios is to obtain the element abundances of main-sequence stars in globular clusters, which are too faint for high resolution spectroscopic studies until now. Both 'evolutionary' and 'primodial' origins are accepted for explanations of abundance variations among red giants and CN-CH anticorrelations among main-sequence stars in globular clusters. This paper reviews chemical abundances of light elements among globular cluster giants, with brief reviews of cannonical stellar evolution of low mass stars after main-sequence and deep mixing for abundance variations of cluster giants, and a possible connection between deep mixing and second parameter.

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Calculation of the Molecular Quadrupole Moments (I). Calculation for the Quadrupole Moment Matrix Elements by Operator Technique (분자의 사중극자모멘트의 계산 (제1보). 연산자법에 의한 사중극자모멘트행렬요소의 계산)

  • Sangwoon Ahn;Jeong Soo Ko
    • Journal of the Korean Chemical Society
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    • v.23 no.5
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    • pp.296-306
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    • 1979
  • Operator technique has been applied for calculation of the quadrupole moment matrix-elements. Master formulas for the quadrupole moment matrix elements for pairs of Slater type, orbitals are derived, one using the expansion method for spherical harmonics and the other the transformed of the quadrupole moment matrix elements into overlap integrals for Mulliken. The numerical values of the quadrupole moment matrix elements evaluated by two methods are in agreement with each other and the calculated quadrupole moment for the ground state of HCl molecule is also in agreement with that of Nesbet.

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Solid-State $^{31}P$ NMR Chemical Shielding Tensors in Binuclear Platinum Diphosphite Complexes

  • 우애자;Leslie G. Butler
    • Bulletin of the Korean Chemical Society
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    • v.17 no.5
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    • pp.457-460
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    • 1996
  • The principal elements of the 31P NMR chemical shielding tensors have been determined for three binuclear platinum diphosphite complexes, K4[Pt2(P2O5H2)4·2H2O ("Pt2"), K4[Pt2(P2O5H2)4Cl2]·2H2O ("Pt2Cl2"), and K4[Pt2(P2O5H2)4Br2]·2H2O ("Pt2Br2"), by using a Herzfeld-Berger graphical method for interpreting the 31P MAS spectrum. The orientations of 31P chemical shielding tensor relative to the molecular axis system are partially assigned with combination of the longitudinal relaxation study of HPO32- and the reference to known tensor orientations of related sites; the most chemical shielding component, δ33, is directed along the P-Pt bond axis. A discussion is given in which the experimental principal elements of the 31P chemical shielding tensor are related with the Pt-Pt bond distances in binuclear platinum diphosphite complexes.