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Artykuły w czasopismach na temat "XANES"
Natori, Sachika, Minako Kurisu, Naomi Kawamura i Yoshio Takahashi. "High-Energy Resolution Fluorescence Detected X-ray Absorption Spectroscopy for the Speciation of Fe in Aerosol Samples". Minerals 12, nr 5 (26.04.2022): 536. http://dx.doi.org/10.3390/min12050536.
Pełny tekst źródłaNatori, Sachika, Minako Kurisu, Naomi Kawamura i Yoshio Takahashi. "High-Energy Resolution Fluorescence Detected X-ray Absorption Spectroscopy for the Speciation of Fe in Aerosol Samples". Minerals 12, nr 5 (26.04.2022): 536. http://dx.doi.org/10.3390/min12050536.
Pełny tekst źródłaNicholls, M., M. N. Najman, Z. Zhang, M. Kasrai, P. R. Norton i P. U. P. A. Gilbert. "The contribution of XANES spectroscopy to tribology". Canadian Journal of Chemistry 85, nr 10 (1.10.2007): 816–30. http://dx.doi.org/10.1139/v07-093.
Pełny tekst źródłaGe, Mingyuan, i Wah-Keat Lee. "PyXAS – an open-source package for 2D X-ray near-edge spectroscopy analysis". Journal of Synchrotron Radiation 27, nr 2 (20.02.2020): 567–75. http://dx.doi.org/10.1107/s1600577520001071.
Pełny tekst źródłaKizler, P., P. Lamparter i S. Steeb. "X -Ray Absorption Near Edge Structure (XANES) Calculations for the Amorphous Fe80B20- and Ni80B20-Alloys". Zeitschrift für Naturforschung A 44, nr 3 (1.03.1989): 189–94. http://dx.doi.org/10.1515/zna-1989-0304.
Pełny tekst źródłaPark, Jae Yeon, Jitendra Pal Singh, Jun Lim i Sangsul Lee. "Development of XANES nanoscopy on BL7C at PLS-II". Journal of Synchrotron Radiation 27, nr 2 (20.02.2020): 545–50. http://dx.doi.org/10.1107/s160057752000082x.
Pełny tekst źródłaPongpiachan, Siwatt, Kanjana Thumanu, Charnwit Kositanont, Klaus Schwarzer, Jörg Prietzel, Phoosak Hirunyatrakul i Itthipon Kittikoon. "Parameters Influencing Sulfur Speciation in Environmental Samples Using Sulfur K-Edge X-Ray Absorption Near-Edge Structure". Journal of Analytical Methods in Chemistry 2012 (2012): 1–12. http://dx.doi.org/10.1155/2012/659858.
Pełny tekst źródłaPrice, S. W. T., K. Ignatyev, K. Geraki, M. Basham, J. Filik, N. T. Vo, P. T. Witte, A. M. Beale i J. F. W. Mosselmans. "Chemical imaging of single catalyst particles with scanning μ-XANES-CT and μ-XRF-CT". Physical Chemistry Chemical Physics 17, nr 1 (2015): 521–29. http://dx.doi.org/10.1039/c4cp04488f.
Pełny tekst źródłaLeri, Alessandra C., i Bruce Ravel. "Sample thickness and quantitative concentration measurements in BrK-edge XANES spectroscopy of organic materials". Journal of Synchrotron Radiation 21, nr 3 (12.03.2014): 623–26. http://dx.doi.org/10.1107/s1600577514001283.
Pełny tekst źródłaRANJAN, RAKESH KUMAR. "Derivation of Relation between a parameter of Inverse correlation and effective Charge of X-ray absorbing K-Edge of Copper atom in it’s different Compounds". Journal of Ultra Scientist of Physical Sciences Section B 32, nr 5 (31.10.2020): 31–35. http://dx.doi.org/10.22147/jusps-b/320501.
Pełny tekst źródłaRozprawy doktorskie na temat "XANES"
Ferrand, Jessica. "Le phénomène de brunissement des vitraux médiévaux : critères d’identification et nature de la phase d’altération". Thesis, Paris Est, 2013. http://www.theses.fr/2013PEST1174/document.
Pełny tekst źródłaThe medieval stained glass windows, which glass composition contain manganese, are often affected by an alteration commonly designated as "browning". This phenomenon results in the presence of Mn-rich brown spots at the surface or subsurface of the glass thus limiting the passage of light and hindering the interpretation of the artwork. Poorly documented, the occurrence of browning among stained glass windows is not precisely described. Currently, one of the major problems in terms of conservation and restoration is that long-term treatments are not available. In these conditions, the recommendations are not to treat the affected glasses, a solution that satisfies neither the architects nor the curators, nor the restorers. In order to answer the questions and expectations of curators and restorers the comprehension of this phenomenon is essential. In this work, a panel of 24 historical and 3 archaeological stained glass samples were studied by microscopic and spectroscopic methods in order to i) establish reliable criteria for identifying the browning phenomenon due to manganese and ii) obtain information on the nature of the dark phases and the oxidation state of manganese in these phases. In parallel with the study of ancient samples, synthetic glasses with medieval-like compositions were synthesized for: i) understanding the reaction between manganese and iron, as well as the influence of the process parameters on the color of glasses and ii) studying the influence of bacteria in the development of the browning phenomenon
Gatuingt, Laure. "Etude des mécanismes de formation des patines manganésifères des grès du château de Lunéville". Thesis, Paris Est, 2017. http://www.theses.fr/2017PESC1085/document.
Pełny tekst źródłaThe formation of iron and/or manganese black patina on sandstone buildings is a phenomenon observed for various environments but which is not fully understood yet. The palace of Lunéville, in eastern France, is an interesting example because it has patinas that have developed in different conditions : some seem to have grown naturally while others have appeared on stones which were exposed to a fire. These stones experienced an increase of their surface temperature, but most of all, they were subjected to a substantial volume of water as part of attempts to extinguish the fire. The goal of this thesis is to understand the formation of the patinas by investigating different sandstone facies collected from the palace of Lunéville and from quarry. In order to understand the influence of the sandstones intrinsic parameters, the patinated and unpatinated facies were compared from petrophysical, chemical and mineralogical point of view, using laboratory techniques (optical and electron microscopy with energy dispersive X-ray spectroscopy, X-ray diffraction, Raman spectrometry, permeability, porosity and capillarity measurements, ...) and large instruments (Particle Induced X-ray Emission (PIXE) on the AGLAE proton accelerator, X-ray micro-diffraction analysis and X-ray absorption micro spectroscopy (XANES) at the SOLEIL synchrotron). In addition to this characterization, patinas coming from different environments were also compared in order to extract the main extrinsic parameters. Finally, the dynamical aspect of the release of manganese from the sandstones was investigated by conducting dissolution experiments at various pH, and by demonstrating the possibility to recreate a Mn patina in laboratory, using sandstone imbibition techniques. The results allow to propose a model for the patina formation based on the dissolution of the Mn-phases initially present in the sandstones’ bulks, followed by the migration through the porous network towards the surface of the ions released in the solution
Mizoguchi, Teruyasu. "Study of Local Atomic and Electronic Structures in Ceramic Materials by ELNES and XANES". 京都大学 (Kyoto University), 2002. http://hdl.handle.net/2433/149775.
Pełny tekst źródłaNemausat, Ruidy. "Etude expérimentale et théorique des fluctuations thermiques quantiques des noyaux par spectroscopies d'absorption X et RMN". Thesis, Paris 6, 2016. http://www.theses.fr/2016PA066158/document.
Pełny tekst źródłaIn this thesis the impact of quantum thermal fluctuations on XANES and solid-state NMR spectra is described using an experimental and theoretical joint study. This project has two components. First, high-quality experimental data are acquired in order to observe and understand the influence of quantum vibrations in light-elements oxides. Second, a theoretical model is set up to reproduce the effects observed experimentally and describe their origin from a fundamental point of view. The developed theoretical approach is based on the density-functional theory. Within the Born-Oppenheimer and quasiharmonic approximations, the quantum thermal fluctuations of nuclei are modeled by generating atomic configurations obeying quantum statistics at finite temperature. The XANES spectra and NMR parameters are subsequently calculated in these configurations and the average results are compared with spectroscopic data at finite temperature. This approach has been validated by a joint theoretical-experimental study conducted in a series of light-element oxides, where the results were found to be in excellent agreement with the original experimental data. In addition, it is shown that the impact of the quantum fluctuations of the nuclei is influenced by the local symmetry of the probed atomic site
Marcaillou, Clément. "Serpentinisation et production d'hydrogène en contexte de dorsale lente : approche expérimentale et numérique". Phd thesis, Université de Grenoble, 2011. http://tel.archives-ouvertes.fr/tel-00676948.
Pełny tekst źródłaPiton, Marcelo Rizzo. "Síntese e caracterização do composto SrTi1-xMnxO3 nanoestruturado". Universidade de São Paulo, 2014. http://www.teses.usp.br/teses/disponiveis/18/18158/tde-29012015-215637/.
Pełny tekst źródłaNanostructured SrTi1-xMnxO3 (STM) powder samples with x = 0%, 0.5%, 1%, 2.5%, 5% and 10% were synthesized by the polymeric precursors method. The thermal, structural and optical properties of STM samples heat-treated at different temperatures were analyzed by thermal analysis, X-ray diffraction, X-ray absorption spectroscopy and photoluminescence techniques. The thermal analysis results have shown that manganese ion causes a retarding effect, increasing the onset of the crystallization temperature. The XRD results showed that manganese ion is incorporated in a solid solution in the B site of the SrTiO3 (ST) network for the range of solubility studied, with oxidation states between +3.4 and +3.7, indicating the creation of charge compensation defects, keeping the materials electrical neutrality. The analysis of the photoluminescence (PL) spectra of the STM amorphous samples showed that the PL intensity increases when the amount of manganese is up to 1%. However, higher manganese concentrations leads to a pronounced decrease of the photoluminescence intensity. The amorphous samples showed no significant change of the local order around the titanium atoms, observed as well as in the oxidation state of the manganese atoms as the amount of manganese increases. Thus, the variation of the photoluminescence intensity cannot be explained by these factors. Increasing the calcination temperature leads to a significant decrease of the photoluminescence intensity. An analysis of the XANES spectra measured at the titanium K edge of these samples showed that as the calcination temperature increases, i. e., as it increases the degree of crystallinity, the ordering of the Ti atoms in the oxygen octahedra TiO6 of the samples increases.
Benali, Cherif Nourredine. "Etude structurale de complexes de cuivre par diffraction et spectroscopie d'absorption X (EXAFS et XANES)". Aix-Marseille 3, 1994. http://www.theses.fr/1994AIX30038.
Pełny tekst źródłaGorczyca, Agnès. "Caractérisation de catalyseurs métalliques supportés par spectroscopie XANES, apports du calcul quantique dans l'interprétation des spectres expérimentaux". Thesis, Grenoble, 2014. http://www.theses.fr/2014GRENI062/document.
Pełny tekst źródłaThe study of metallic nanoclusters supported on oxides is of paramount fundamental and technological importance, particularly in the field of energy. The nanoparticles based on platinum supported on gamma alumina are widely used as highly dispersed heterogeneous catalysts especially under reducing hydrogen atmosphere. Their reactivity and selectivity are intimately related to the local geometry and the electronic density of active sites. These are particularly difficult to define, given the very small size of the studied particles (about 0.8 nm in diameter). XANES (X-Ray Absorption Near Edge Structure) spectroscopy requiring synchrotron radiation, is one of the most appropriate tools to study these systems, especially in situ, at the atomic scale. Indeed the XANES spectra are influenced by the geometry and symmetry of the atoms local environment (especially angles between bonds), the degree of oxidation, the bond types involved, and the electronic structure of the system . All these factors are nevertheless difficult to differentiate and even to interpret. It is therefore impossible to infer accurately the structure of the metal particles by experience alone, without any comparison with simulated spectra. The establishment of theoretical models becomes necessary. We are implementing an approach that combines high-resolution XANES experiments in situ and quantum simulations, the latter aimed at proposing relevant structural models to quantify the reactivity of the particles and calculating spectral characteristics for comparison to experiment. The identification of the clusters morphologies, the metal-support interaction and the hydrogen coverage is made possible combining experiments and quantum calculations. The library of existing monometallic Pt particles models supported on Gamma alumina with or without adsorbed hydrogen, is refined. New models considering the two main surface of Gamma alumina, the particle size and hydrogen adsorption are developed. This extended library of models enabled a study of the effect of particle size, morphology, electronic structure, different alumina faces, and the hydrogen coverage on the signature of XANES spectra. This first study of monometallic platinum catalysts, concludes with the discrimination of the morphologies, but especially with the quantification of the hydrogen coverage of the particles for each temperature and hydrogen pressure experimental condition. Then, models of bimetallic Platinum-tin particles supported on the (100) Gamma alumina face are performed with hydrogen adsorption. These models provide insights into the effect of tin on the morphology, the electronic properties and the interaction with the support and hydrogen of these clusters. Different compositions were explored, which provided information on the dilution of platinum by tin. The adsorption of hydrogen was then studied on Pt10Sn3 clusters supported on the (100) face of alumina. Although many parameters are not yet included in these models, the comparison to the experience already provides a first approximation to the description of bimetallic systems
Fernandes, Alessandro. "Síntese e caracterização do composto SrTi1-XNbXO3 nanoestruturado". Universidade de São Paulo, 2012. http://www.teses.usp.br/teses/disponiveis/88/88131/tde-15082012-125906/.
Pełny tekst źródłaNanostructured \'SR\'TI IND.1-x\'NB IND.x\'O IND.3\' samples in a powder form containing up to 10 mol% of niobium have been prepared by the polymeric precursor method. The thermal, structural and optical properties of these samples were characterized by different techniques. The results show that in the limit of concentration of niobium added to the samples, the dopant was incorporated into the \'SR\'TI\'O IND.3\' matrix lattice forming a \'SR\'TI IND.1-x\'NB IND.x\'O IND.3\' solid solution. The increasing on the amount of niobium leads to an increased agglomeration of the particles as well as an increase in the crystallization temperature of the samples. In good agreement with the literature data, a significant photoluminescence intensity was only observed in amorphous or partially crystalline samples. Samples in the form of thin films were obtained using the electron beam evaporation technique. X-ray diffraction (XRD) show that in certain compositions, beyond the \'SR\'TI\'O IND.3\' phase, it was also observed the presence of phase \'SR\'CO IND.3\' phase. Through the XRD and Atomic Force Microscope (AFM) results, it has been observed that, as in the case of the samples in powder form, the concentration of niobium inhibits the crystallization process of the sample. Electrical resistance measurements showed that all samples, independent of the concentration of niobium, present higher values of resistance of the order of \'10 POT.15\' \'ômega\' . This value is much higher than expected and reported in the literature and does not allowed to measure the sensibility of thin films to different species of gases.
Santos, Sheila Renata. "Dinâmica do fósforo no solo em função da adição de ácidos orgânicos de baixa massa molar". Universidade de São Paulo, 2016. http://www.teses.usp.br/teses/disponiveis/11/11140/tde-10052016-131749/.
Pełny tekst źródłaPhosphate fertilization of acidic, highly weathered soils is inefficient because of the adsorption of phosphorus (P) to 1:1 silicate clays and, especially, to Fe and Al oxides. Different soil management practices to induce solubilization of unavailable forms of P to plants nutrition have been intensively studied in recent years. The mobilization of P with anions of low molecular weight organic acids (LMWOA) increases the concentration of available P in the soil solution for plant uptake. Anions derived from LMWOA exudates from plants root or excreted by microbes are associated with some rhizosphere conditions, as deficiency of P and Al phytotoxicity, and they interact with the soil in order to increase P availability. Depending on the soil attributes, and degree of dissociation, properties, and number of carboxyl groups from organic anions, P can be mobilized from soil mainly because of complexometric dissolution of soil minerals and ligand exchange of functional carboxyl groups and P adsorbed in soil surface sites. The capacity of citrate, malate and oxalate anions to mobilize P from a Typic Quartzipsamment (RQ) and an Anionic Acrudox (LVwf) was evaluated in a column leaching study. Because no P was detectable in columns effluents from LVwf, another column leaching study was performed, but only citrate was leached with a greater volume of solution, and citrate-induced changes at P forms in the soil were identified by P K-edge X-ray absorption near edge structure - XANES - spectroscopy. The capacity of LMWOA anions to solubilize P was more dependent of P status and other soil attributes, than number of carboxyl groups of organic anions. Only oxalate mobilized P from RQ, and all LMWOA anions were able to mobilize P from LVwf. Increasing of P mobilization and soil pH were followed by increases of Al mobilization from RQ (pH water = 5), and Ca mobilization from LVwf (pH water = 5.6) at lower volumes of LMWOA anions leaching. Phosphorus was solubilized by complexation of Al, Ca or Fe from insoluble phosphate minerals, or by inhibition of Al, Ca or Fe phosphate precipitation. After leaching a greater volume of citrate through LVwf, P was still undetectable in effluents from columns, but there was an intensively leaching of Al and Fe, as well as changes in proportions of adsorbed P characterized in soil XANES spectra. Although we have found evidences about the action of main mechanisms of P solubilization (complexometric dissolution, and ligand exchange of carboxylic functional groups for adsorbed P on soil minerals) by LMWOA anions, they had a little potential to really increase P availability.
Książki na temat "XANES"
F, Hepp Aloysius, i United States. National Aeronautics and Space Administration., red. XANES and EXAFS study of Au-substituted YBBa₂Cu₃O₇-[delta]. Washington, DC: National Aeronautics and Space Administration, 1990.
Znajdź pełny tekst źródłaC, Koningsberger D., i Prins Roelof, red. X-ray absorption: Principles, applications, techniques of EXAFS, SEXAFS, and XANES. New York: Wiley, 1988.
Znajdź pełny tekst źródłaKizler, Peter. Untersuchung der dreidimensionalen Struktur der amorphen Legierung Fe80B20 [Fe-B] anhand von Strukturmodellen mit Hilfe der XANES-Spektroskopie. [s.l.]: [s.n.], 1988.
Znajdź pełny tekst źródłaJavaxišvili, Giorgi. Adrepʻeodaluri xanis kʻartʻuli stelebi. Tʻbilisi: Tʻbilisis universitetis gamomcʻemloba, 1998.
Znajdź pełny tekst źródłaTʻbilisis saxelmcipʻo universiteti. Sakʻartʻvelos istoriis instituti, red. Pʻeodaluri xanis Sakʻartʻvelos ekonomikuri istoria. Tʻbilisi: Gamomcʻemloba "Kolori", 2020.
Znajdź pełny tekst źródłaCerasuolo, Omar. Xanaes: Poesía, canciones y otros relatos. Bs. As. [i.e. Buenos Aires]: Corregidor, 1991.
Znajdź pełny tekst źródłaMargiašvili, S. Antikur xanis mdidruli samarxebi Algetʻis xeobidan. Tʻbilisi: Mecʻniereba, 1992.
Znajdź pełny tekst źródłaNioraże, Medea. Żveli kʻvis xanis mġvime-namosaxlarebi Cqalcitʻelas xeobaši. Tʻbilisi: "Mecʻniereba", 1992.
Znajdź pełny tekst źródłaBerżnišvili, Mamisa. Pʻeodaluri xanis Sakʻartʻvelos istoriis cerilobitʻi cqaroebi: Cqarotʻmcʻodneobitʻi gamokvlevebi. Tʻbilisi: Mecnʻiereba, 1989.
Znajdź pełny tekst źródłaVašakiże, V. Elinisturi xanis Kʻartʻlis samepʻos socʻialuri istoriidan: Istoriul-cqarotʻmcʻodneobitʻi gamokvleva. Tʻbilisi: Mecʻniereba, 1991.
Znajdź pełny tekst źródłaCzęści książek na temat "XANES"
Cleaves, Henderson James. "XANES". W Encyclopedia of Astrobiology, 1781. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-11274-4_1693.
Pełny tekst źródłaCleaves, Henderson James. "XANES". W Encyclopedia of Astrobiology, 2657. Berlin, Heidelberg: Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-662-44185-5_1693.
Pełny tekst źródłaCleaves, Henderson James. "XANES". W Encyclopedia of Astrobiology, 1. Berlin, Heidelberg: Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-27833-4_1693-4.
Pełny tekst źródłaCleaves, Henderson James. "XANES". W Encyclopedia of Astrobiology, 1. Berlin, Heidelberg: Springer Berlin Heidelberg, 2022. http://dx.doi.org/10.1007/978-3-642-27833-4_1693-5.
Pełny tekst źródłaCleaves, Henderson James. "XANES". W Encyclopedia of Astrobiology, 3255. Berlin, Heidelberg: Springer Berlin Heidelberg, 2023. http://dx.doi.org/10.1007/978-3-662-65093-6_1693.
Pełny tekst źródłaCramer, Stephen P. "XANES and XMCD". W X-Ray Spectroscopy with Synchrotron Radiation, 165–90. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-28551-7_7.
Pełny tekst źródłaBauch, Jürgen, i Rüdiger Rosenkranz. "EXAFS / XANES - Röntgenabsorptionsspektroskopie". W Physikalische Werkstoffdiagnostik, 70–71. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-53952-1_35.
Pełny tekst źródłaGarcía Ruiz, Joaquín. "Local Geometry by XANES and RXS". W Springer Proceedings in Physics, 345–50. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-73811-6_22.
Pełny tekst źródłaShimomura, Osamu, i Takaaki Kawamura. "EXAFS and XANES study under pressure". W High‐Pressure Research in Mineral Physics: A Volume in Honor of Syun‐iti Akimoto, 187–93. Washington, D. C.: American Geophysical Union, 1987. http://dx.doi.org/10.1029/gm039p0187.
Pełny tekst źródłaHasnain, S. Samar. "EXAFS and XANES Studies of Copper Proteins". W Biophysics and Synchrotron Radiation, 147–58. Berlin, Heidelberg: Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-642-71490-0_18.
Pełny tekst źródłaStreszczenia konferencji na temat "XANES"
Metzler, Rebecca A., Ronke M. Olabisi, Mike Abrecht, Daniel Ariosa, Christopher J. Johnson, Benjamin Gilbert, Bradley H. Frazer, Susan N. Coppersmith i P. U. P. A. Gilbert. "XANES in Nanobiology". W X-RAY ABSORPTION FINE STRUCTURE - XAFS13: 13th International Conference. AIP, 2007. http://dx.doi.org/10.1063/1.2644429.
Pełny tekst źródłaBiegert, Jens. "Attosecond water-window XANES". W Ultrafast Phenomena and Nanophotonics XXV, redaktorzy Markus Betz i Abdulhakem Y. Elezzabi. SPIE, 2021. http://dx.doi.org/10.1117/12.2577019.
Pełny tekst źródłaRau, Christoph, Andrea Somogyi, A. Bytchkov i Alexandre S. Simionovici. "XANES micro-imaging and tomography". W International Symposium on Optical Science and Technology, redaktor Ulrich Bonse. SPIE, 2002. http://dx.doi.org/10.1117/12.452851.
Pełny tekst źródłaMiller, Nicholas A., i Roseanne J. Sension. "Polarized XANES Elucidate Femtosecond Bond Elongation". W Laser Science. Washington, D.C.: OSA, 2017. http://dx.doi.org/10.1364/ls.2017.lm2f.2.
Pełny tekst źródłaZhang, Z., E. S. Yamaguchi, M. Kasrai, G. M. Bancroft, X. Liu i M. E. Fleet. "Tribofilms Generated From ZDDP and DDP on Steel Surfaces: Part 2 — Chemistry". W World Tribology Congress III. ASMEDC, 2005. http://dx.doi.org/10.1115/wtc2005-63251.
Pełny tekst źródłaHarris, William M., George J. Nelson, John R. Izzo, Kyle N. Grew, Wilson K. S. Chiu, Yong S. Chu, Jaemock Yi, Joy Andrews, Yijin Liu i Piero Pianetta. "Full Field Imaging of Nickel Oxidation States in Solid Oxide Fuel Cell Anode Materials by Xanes Nanotomography". W ASME 2011 9th International Conference on Fuel Cell Science, Engineering and Technology collocated with ASME 2011 5th International Conference on Energy Sustainability. ASMEDC, 2011. http://dx.doi.org/10.1115/fuelcell2011-54947.
Pełny tekst źródłaLobacheva, O., L. V. Goncharova, M. Chavarha i T. K. Sham. "XANES study of Fe-implanted strontium titanate". W ELECTRONIC, PHOTONIC, PLASMONIC, PHONONIC AND MAGNETIC PROPERTIES OF NANOMATERIALS. AIP Publishing LLC, 2014. http://dx.doi.org/10.1063/1.4870200.
Pełny tekst źródłaArcovito, Alessandro, Maurizio Benfatto, Paola D’Angelo i Stefano Della Longa. "Hemeproteins: Recent Advances in Quantitative XANES Analysis". W X-RAY ABSORPTION FINE STRUCTURE - XAFS13: 13th International Conference. AIP, 2007. http://dx.doi.org/10.1063/1.2644508.
Pełny tekst źródłaPhilippon, D., M. I. De Barros, Th Le Mogne, J. M. Martin i M. Kasrai. "Friction-Induced Change of Boron Hybridization in Lubricant Additives". W World Tribology Congress III. ASMEDC, 2005. http://dx.doi.org/10.1115/wtc2005-64188.
Pełny tekst źródłaPattammattel, Ajith, Ryan Tappero, Mingyuan Ge, Yong Chu, Xiaojing Huang, Yuan Gao i Hanfei Yan. "Nano-XANES: Chemical Mapping with Hard X-Rays". W Goldschmidt2020. Geochemical Society, 2020. http://dx.doi.org/10.46427/gold2020.2044.
Pełny tekst źródłaRaporty organizacyjne na temat "XANES"
Myneni, S. C. B., i R. C. C. Perera. Ca and S K-edge XANES studies of calcite-acid mine water interactions. Office of Scientific and Technical Information (OSTI), kwiecień 1997. http://dx.doi.org/10.2172/603631.
Pełny tekst źródłaRobblee, John Henry. XANES, EXAFS and Kbeta spectroscopic studies of the oxygen-evolving complex in Photosystem II. Office of Scientific and Technical Information (OSTI), grudzień 2000. http://dx.doi.org/10.2172/773946.
Pełny tekst źródłaBrown, J. R., M. Kasrai, G. M. Bancroft, C. M. White i K H Tan. Fingerprinting sulfur forms in coal and coal macerals using sulfur l-edge XANES validation of classical methodology. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 1992. http://dx.doi.org/10.4095/304540.
Pełny tekst źródłaPalmer, S. R., i G. P. Huffman. Analyzing organic sulfur in coal/char: Integrated mild gasification/XANES methods. Technical report, 1 March--31 May 1994. Office of Scientific and Technical Information (OSTI), wrzesień 1994. http://dx.doi.org/10.2172/10183105.
Pełny tekst źródłaDel Grande, N. L shell XANES (x-ray absorption near edge structure) for solid metals: Ti, V, Cr, Fe, Ni, Cu. Office of Scientific and Technical Information (OSTI), styczeń 1990. http://dx.doi.org/10.2172/7253344.
Pełny tekst źródłaSchmuki, P., S. Virtanen, H. Boehni, H. S. Isaacs, M. P. Ryan i L. J. Oblonsky. In situ XANES study of the cathodic reduction behavior of the passive film on iron and artificial passive films. Office of Scientific and Technical Information (OSTI), październik 1997. http://dx.doi.org/10.2172/537262.
Pełny tekst źródłaPalmer, S. R., i G. P. Huffman. Analyzing organic sulfur in coal/char: Integrated mild degradation/XANES methods. [Quarterly] technical report, September 1--November 30, 1993. Office of Scientific and Technical Information (OSTI), grudzień 1993. http://dx.doi.org/10.2172/10133861.
Pełny tekst źródłaO'Day, P., S. A. Carroll i S. Bajt. Comparison of Synchrotron X-Ray Fluorescence Mapping and Micro-XANES to Bulk X-Ray Absorption Spectra in Metal-Contaminated Sediments. Office of Scientific and Technical Information (OSTI), styczeń 2003. http://dx.doi.org/10.2172/15007217.
Pełny tekst źródłaPalmer, S. R., i G. P. Huffman. Analyzing organic sulfur in coal/char: Integrated mild degradation/XANES methods. [Quarterly] technical report, December 1, 1993--February 28, 1994. Office of Scientific and Technical Information (OSTI), czerwiec 1994. http://dx.doi.org/10.2172/10154276.
Pełny tekst źródłaChaturvedi, S., J. A. Rodriguez, J. C. Hanson, A. Albornoz i J. L. Brito. Properties of pure and sulfided NiMoO{sub 4} and CoMoO{sub 4} catalysts: TPR, XANES and time-resolved XRD studies. Office of Scientific and Technical Information (OSTI), grudzień 1998. http://dx.doi.org/10.2172/555287.
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