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      • SCISCIESCOPUS

        Spectroscopic and molecular characterization of humic substances (HS) from soils and sediments in a watershed: comparative study of HS chemical fractions and the origins

        Derrien, M.,Lee, Y. K.,Park, J. E.,Li, P.,Chen, M.,Lee, S. H.,Lee, S. H.,Lee, J. B.,Hur, J. Springer Science + Business Media 2017 Environmental Science and Pollution Research Vol.24 No.20

        <P>Optical properties and molecular composition of humic substances (HS) can provide valuable information on the sources and the history of the associated biogeochemical processes. In this study, many well-known spectral and molecular characteristics were examined in eight different HS samples, which were extracted from soils and sediments located in a forested watershed, via two advanced tools including fluorescence excitation emission matrix-parallel factor analysis (EEM-PARAFAC) and high-resolution Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR MS). Two humic-like (C1 and C2) and one protein-like (C3) components were identified from EEM-PARAFAC. Irrespective of the origins, humic acid (HA) fractions were distinguished from fulvic acid (FA) fractions by the HS characteristics of specific UV absorbance (SUVA), the number of formulas, maximum fluorescence intensities of C1 and C2, condensed aromatics, tannins, and CHON, CHOS, and CHONS classes. In contrast, only five HS indices, including C3 intensity, H%, modified aromatic index (AI(mod)), the percentages of carbohydrates, and unsaturated hydrocarbons, were found to be significant factors in discriminating between the two HS origins (i.e., soils and sediments). The ordination of the Bray-Curtis dissimilarity matrix further confirmed that the HS chemical fraction (i.e., HA or FA) was the more important factor to determine the measured HS characteristics than the HS origin. Our results provided an in-depth insight into the chemical and structural heterogeneity of bulk HS, which could be even beyond the differences observed along the two HS origins. This study also delivers a cautious message that the two operationally defined HS chemical fractions should be carefully considered in tracking the origins of different HS samples.</P>

      • KCI등재

        Evaluation of the Chromium Resonance Parameters Including Resonance Parameter Covariance

        L. Leal,H. Derrien,K. Guber,G. Arbanas,D. Wiarda 한국물리학회 2011 THE JOURNAL OF THE KOREAN PHYSICAL SOCIETY Vol.59 No.23

        The intent of this work is to report the results and describe the procedures utilized to evaluate the chromium isotopes' cross sections, i.e., ^(50)Cr, ^(52)Cr, ^(53)Cr, and ^(54)Cr, for criticality safety applications. The evaluations were done in the resolved resonance region using the reduced Reich-Moore R-matrix formalism. The novel aspect of this evaluation is the inclusion of new transmission and capture cross-section measurements performed at the Oak Ridge Electron Linear Accelerator (ORELA) for energies below 100 keV and the extension of the ^(53)Cr energy region. The resonance analysis was performed with the multilevel R-matrix code, SAMMY, which utilizes the generalized least-squares technique based on the Bayes' theory. Complete sets of resonance parameters and resonance parameter covariance matrices (RPCMs) were obtained for each of the chromium isotopes from the SAMMY analysis of the experimental database.

      • KCI등재

        Resonance Region Nuclear Data Analysis to Support Advanced Fuel Cycle Development

        M. E. Dunn,H. Derrien,L. C. Leal,C. Gil,김도헌 한국물리학회 2011 THE JOURNAL OF THE KOREAN PHYSICAL SOCIETY Vol.59 No.23

        The Oak Ridge National Laboratory (ORNL) and the Korean Atomic Energy Research Institute (KAERI) are performing collaborative research as part of a three-year United States (U.S.)-Republic of Korea (ROK) International Nuclear Energy Research Initiative (I-NERI) project to provide improved neutron cross-section data with uncertainty or covariance data important for advanced fuel cycle and nuclear safeguards applications. ORNL and KAERI have initiated efforts to prepare new cross-section evaluations for ^(240)Pu, ^(237)Np, and the stable Cm isotopes. At the current stage of the I-NERI project, ORNL has recently completed a preliminary resonance-region cross-section evaluation with covariance data for ^(240)Pu and has initiated resonance evaluation efforts for ^(237)Np and ^(244)Cm. Likewise, KAERI is performing corresponding high-energy cross-section analyses (i.e., above the resonance region) for the noted isotopes. The paper provides results pertaining to the new resonance region evaluation efforts with emphasis on the new ^(240)Pu evaluation.

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