Auswahl der wissenschaftlichen Literatur zum Thema „Modélisation de la complexation de surface“
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Zeitschriftenartikel zum Thema "Modélisation de la complexation de surface"
Katz, Lynn E., und Kim F. Hayes. „Surface Complexation Modeling“. Journal of Colloid and Interface Science 170, Nr. 2 (März 1995): 477–90. http://dx.doi.org/10.1006/jcis.1995.1127.
Der volle Inhalt der QuelleKatz, Lynn E., und Kim F. Hayes. „Surface Complexation Modeling“. Journal of Colloid and Interface Science 170, Nr. 2 (März 1995): 491–501. http://dx.doi.org/10.1006/jcis.1995.1128.
Der volle Inhalt der QuelleLudwig, Christian, und Paul W. Schindler. „Surface Complexation on TiO2“. Journal of Colloid and Interface Science 169, Nr. 2 (Februar 1995): 284–90. http://dx.doi.org/10.1006/jcis.1995.1035.
Der volle Inhalt der QuelleLudwig, Christian, und Paul W. Schindler. „Surface Complexation on TiO2“. Journal of Colloid and Interface Science 169, Nr. 2 (Februar 1995): 291–99. http://dx.doi.org/10.1006/jcis.1995.1036.
Der volle Inhalt der QuelleDyrssen, David. „Sulfide complexation in surface seawater“. Marine Chemistry 24, Nr. 2 (Juni 1988): 143–53. http://dx.doi.org/10.1016/0304-4203(88)90045-x.
Der volle Inhalt der QuelleForsling, Willis, und Liuming Wu. „Surface complexation at hydrous fluorapatite“. Aquatic Sciences 55, Nr. 4 (1993): 336–46. http://dx.doi.org/10.1007/bf00877278.
Der volle Inhalt der QuelleBelhamri, Azeddine, und Jean Paul Fohr. „Influence de l’Evolution de l’Etat de Surface sur la Modèlisation du Séchage de Milieux Poreux“. Journal of Renewable Energies 1, Nr. 1 (30.06.1998): 29–35. http://dx.doi.org/10.54966/jreen.v1i1.941.
Der volle Inhalt der QuelleErzuah, Samuel, Ingebret Fjelde und Aruoture V. Omekeh. „Wettability Estimation Using Surface-Complexation Simulations“. SPE Reservoir Evaluation & Engineering 22, Nr. 02 (01.05.2019): 509–19. http://dx.doi.org/10.2118/185767-pa.
Der volle Inhalt der QuelleTraina, S. J. „Surface complexation modeling: Hydrous ferric oxide“. Geochimica et Cosmochimica Acta 60, Nr. 21 (November 1996): 4291. http://dx.doi.org/10.1016/s0016-7037(97)81467-6.
Der volle Inhalt der QuelleMorgan, J. J. J. „Surface complexation modeling: Hydrous ferric oxide“. Journal of Colloid and Interface Science 141, Nr. 2 (Februar 1991): 595–96. http://dx.doi.org/10.1016/0021-9797(91)90361-b.
Der volle Inhalt der QuelleDissertationen zum Thema "Modélisation de la complexation de surface"
Devau, Nicolas. „Processus rhizosphériques déterminant la disponibilité en phosphore : apport de la modélisation mécaniste géochimique“. Thesis, Montpellier, SupAgro, 2010. http://www.theses.fr/2010NSAM0019.
Der volle Inhalt der QuelleRoot-induced chemical processes are recognized as a major strategy developed by plants to enhance phosphorus (P) availability and thus to promote P acquisition. However, the exact influence of these root-induced chemical processes is still poorly understood and quantified. The present study aimed at investigating the influence of root-induced chemical processes, especially root-induced pH changes, on P availability in the rhizosphere. In this work, we used a set of mechanistic adsorption models (« 1-pK triple plane », ion-exchange and Nica-Donnan) within the framework of the component additive approach in order to simulate the effects of root activity on P availability. First, we described the effects of pH on P availability in several soils unaffected by roots, a Chromic Cambisol and a Luvisol. The Luvisol showed different concentrations in inorganic P because of a long-term fertilisation trial. In the rhizosphere of durum wheat (Triticum tu rgidum durum L.) grown on these two soils, we found that calcium (Ca) uptake, in addition to P uptake and root-induced alkalisation, controlled to various extents the changes of soil P availability. Calcium uptake markedly increased P availability by decreasing the promoting effect of Ca adsorption on P adsorption. The relative influence of these three root processes depended on the solution composition (especially concentration of Ca and pH). Our simulations showed the relationship between changes in P availability and the speciation of adsorbed P onto the different soil minerals. Soil mineralogy, especially the relative abundance of illite vs. Fe oxides, controlled the influence of root processes by regulating the contribution of soil minerals to P adsorption. By identifying a novel root-induced processes, namely the Ca uptake, and describing its influence on P availability, our results demonstrate the ability of surface complexation models to predict the effects of root-i nduced processes on P availability in soils
Naveau, Aude. „Etude et modélisation de la sorption d'ions à la surface de sulfures métalliques en conditions de stockage en milieu géologique profond“. Reims, 2005. http://theses.univ-reims.fr/exl-doc/GED00000168.pdf.
Der volle Inhalt der QuelleThe storage of high-level nuclear wastes in a geological disposal is based on the concept of confinement by a multibarrier system. Transport by groundwaters is the most likely means for radionuclides to migrate through the engineered and geological barriers. Understanding processes which could delay this migration is therefore fundamental to ensure the timelessness of a deep geological repository. The present study was initiated to investigate sorption processes between sulfides minerals, present as inclusions in temperate soils, and two long-life fission products, iodine and selenium. All experiments were performed in strict anoxic conditions in order to prevent the studied solids (pyrite FeS2 and chalcopyrite CuFeS2) from oxidation. Potentiometric studies showed a weak reactivity of the metallic sulfides surfaces attributed to a low specific surface. Sorption experiments showed no affinity between iodide and metallic sulfides surfaces whereas selenium was well retained by the differents solids. Spectroscopic studies (XPS and XANES) showed a reduction of SeIV to Se-II on the sulfide surfaces. Selenium behaviour was finally described with the diffuse layer model using the surface complexation theory
Tertre, Emmanuel. „Adsorption de Cs+, Ni2+ et des lanthanides sur une kaolinite et une smectite jusqu'à 150°C : étude expérimentale et modélisation“. Toulouse 3, 2005. http://www.theses.fr/2005TOU30108.
Der volle Inhalt der QuelleThe motivation for this study is to assess the temperature effect on the clay minerals sorption properties. Sorption and desorption of Cs+, Ni2+ et Ln3+ onto a montmorillonite and a kaolinite were performed by batch experiments between 25 and 150°C, and in different pH and ionic strengths conditions. Sorption enthalpies varying between 0 and 80kJ/mol were then calculated. For europium, surface spectroscopic analyses confirmed that the mechanism involved is adsorption, including at 150°C. Moreover, this method allowed us to obtain qualitatively the different adsorption equilibrium occurring during the reaction. An acid/base study of the clay surfaces was performed in order to assess the temperature effect on the surface charge of these minerals. Then, a surface complexation model including edge sites and structural sites was proposed to interpret the acid/base data and the europium sorption data
Gao, Pengyuan. „Theoretical Studies of the Interaction between U(VI) and Mineral Surfaces“. Electronic Thesis or Diss., Orléans, 2023. http://www.theses.fr/2023ORLE1074.
Der volle Inhalt der QuelleStudies of the adsorption characteristics of key radionuclides in the host rock and buffer/backfill materials of deep geological repositories for high-level waste (HLW) are fundamental to the designand safety assessment. Uranium is a radionuclide of widespread interest due to its relatively high abundance in nature and its central role in the nuclear fuel cycle, while U(VI) is the most relevant oxidation state in most surface waters and oxygenated groundwater. The adsorption of U(VI) on the surfaces of various minerals has been extensively investigated by conventional batch experimentsand spectroscopic techniques. Possible complexation sites and surface species have been proposed,but it is still challenging to able to obtain mechanistically precise insights at the microscopic level.Information at the molecular level is essential to understand the physicochemical mechanisms involved in the experiments and to develop predictive models for the relevant environments.Theoretical computations have been proven to be an effective tool for studying the chemical processesof radionuclides at the mineral-water interface. In this thesis, the structural characteristics and adsorption mechanisms of U(VI) species on the surfaces of the main component minerals of granite(orthoclase and quartz) and buffer/backfill materials (montmorillonite) of the deep geological repository were calculated by first-principles calculations. The polymerization mechanisms of U(VI) species in aqueous solution and on mineral surfaces were investigated. In addition, the effect of local structural changes of montmorillonite on the nature of the adsorption reaction on the surface was also systematically investigated
Emmanuel, Tertre. „Modélisation des propriétés d'adsorption des minéraux argileux gonflants vis-à-vis de cations inorganiques“. Habilitation à diriger des recherches, Université de Poitiers, 2014. http://tel.archives-ouvertes.fr/tel-00984348.
Der volle Inhalt der QuelleBengtsson, Åsa. „Solubility and Surface Complexation Studies of Apatites“. Doctoral thesis, Umeå universitet, Kemi, 2007. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-1408.
Der volle Inhalt der QuelleBengtsson, Åsa. „Solubility and surface complexation studies of apatites /“. Umeå : Department of Chemistry, Umeå University, 2007. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-1408.
Der volle Inhalt der QuelleWu, Liuming. „Surface complexation at calcium mineral-water interfaces“. Doctoral thesis, Luleå, 1994. http://urn.kb.se/resolve?urn=urn:nbn:se:ltu:diva-25727.
Der volle Inhalt der QuelleGodkänd; 1994; 20070429 (ysko)
Taillon, Kate. „Modeling surface complexation relationships in forest and agricultural soil“. Thesis, McGill University, 2005. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=82435.
Der volle Inhalt der QuelleGisler, Thomas. „From surface complexation models to dressed colloidal particles : experiments and theory /“. [S.l.] : [s.n.], 1995. http://e-collection.ethbib.ethz.ch/show?type=diss&nr=11042.
Der volle Inhalt der QuelleBücher zum Thema "Modélisation de la complexation de surface"
Karamalidis, Athanasios K., und David A. Dzombak. Surface Complexation Modeling. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2010. http://dx.doi.org/10.1002/9780470642665.
Der volle Inhalt der QuelleJohannes, Lützenkirchen, Hrsg. Surface complexation modelling. Amsterdam: Elsevier/Academic Press, 2006.
Den vollen Inhalt der Quelle findenA, Dzombak David, Hrsg. Surface complexation modeling: Gibbsite. Hoboken, N.J: Wiley, 2010.
Den vollen Inhalt der Quelle findenDzombak, David A. Surface complexation modeling: Hydrous ferric oxide. New York: Wiley, 1990.
Den vollen Inhalt der Quelle findenHarvey, K. B. Surface-complexation models for sorption onto heterogeneous surfaces. Pinawa, Man: Whiteshell Laboratories, 1997.
Den vollen Inhalt der Quelle findenB, Kent Douglas, U.S. Nuclear Regulatory Commission. Office of Nuclear Material Safety and Safeguards. Division of High-Level Waste Management., Stanford University. Dept. of Civil Engineering. und Sandia National Laboratories, Hrsg. Surface-complexation modeling of radionuclide adsorption in subsurface environments. Washington, DC: Division of High-Level Waste Management, Office of Nuclear Material Safety and Safeguards, U.S. Nuclear Regulatory Commission, 1988.
Den vollen Inhalt der Quelle findenB, Kent Douglas, U.S. Nuclear Regulatory Commission. Office of Nuclear Material Safety and Safeguards. Division of High-Level Waste Management., Stanford University. Dept. of Civil Engineering. und Sandia National Laboratories, Hrsg. Surface-complexation modeling of radionuclide adsorption in subsurface environments. Washington, DC: Division of High-Level Waste Management, Office of Nuclear Material Safety and Safeguards, U.S. Nuclear Regulatory Commission, 1988.
Den vollen Inhalt der Quelle finden1953-, Hayes Kim F., U.S. Nuclear Regulatory Commission. Division of Low-Level Waste Management and Decommissioning. und Stanford University. Dept. of Civil Engineering., Hrsg. Application of surface complexation models for radionuclide adsorption: Sensitivity analysis of model input parameters. Washington, D.C: Division of Low-Level Waste Management and Decommissioning, Office of Nuclear Material Safety and Safeguards, U.S. Nuclear Regulatory Commission, 1990.
Den vollen Inhalt der Quelle finden1953-, Hayes Kim F., U.S. Nuclear Regulatory Commission. Division of Low-Level Waste Management and Decommissioning. und Stanford University. Dept. of Civil Engineering., Hrsg. Application of surface complexation models for radionuclide adsorption: Sensitivity analysis of model input parameters. Washington, D.C: Division of Low-Level Waste Management and Decommissioning, Office of Nuclear Material Safety and Safeguards, U.S. Nuclear Regulatory Commission, 1990.
Den vollen Inhalt der Quelle findenSu, Pu-chʻing. Computational geometry--curve and surface modeling. Boston: Academic Press, 1989.
Den vollen Inhalt der Quelle findenBuchteile zum Thema "Modélisation de la complexation de surface"
Sun, Z. X., und W. Forsling. „Mineral Surface Complexation in Flotation“. In Innovations in Flotation Technology, 263–81. Dordrecht: Springer Netherlands, 1992. http://dx.doi.org/10.1007/978-94-011-2658-8_11.
Der volle Inhalt der QuelleAnderson, Paul R., und Mark M. Benjamin. „Constant-Capacitance Surface Complexation Model“. In ACS Symposium Series, 272–81. Washington, DC: American Chemical Society, 1990. http://dx.doi.org/10.1021/bk-1990-0416.ch021.
Der volle Inhalt der QuelleSchindler, P. W., und G. Sposito. „Surface Complexation at (Hydr)Oxide Surfaces“. In Interactions at the Soil Colloid — Soil Solution Interface, 115–45. Dordrecht: Springer Netherlands, 1991. http://dx.doi.org/10.1007/978-94-017-1909-4_4.
Der volle Inhalt der QuelleMu, Q. S., Y. H. Ma, A. L. Lewis, S. P. Armes und J. R. Lu. „Complexation of DNA with biocompatible diblock copolymers“. In Surface and Colloid Science, 199–202. Berlin, Heidelberg: Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/b97072.
Der volle Inhalt der QuelleSposito, Garrison. „Surface Complexation of Metals by Natural Colloids“. In Ion Exchange and Solvent Extraction, 211–36. Taylor & Francis Group, 6000 Broken Sound Parkway NW, Suite 300, Boca Raton, FL 33487-2742: CRC Press, 2017. http://dx.doi.org/10.4324/9780203749753-5.
Der volle Inhalt der QuelleDavis, J. A., und D. B. Kent. „CHAPTER 5. SURFACE COMPLEXATION MODELING IN AQUEOUS GEOCHEMISTRY“. In Mineral-Water Interface Geochemistry, herausgegeben von Michael F. Hochella und Art F. White, 177–260. Berlin, Boston: De Gruyter, 1990. http://dx.doi.org/10.1515/9781501509131-009.
Der volle Inhalt der QuelleSherman, David M., Chris G. Hubbard und Caroline L. Peacock. „Surface complexation of U(VI) by Fe and Mn (hydr)oxides“. In Uranium, Mining and Hydrogeology, 929–30. Berlin, Heidelberg: Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-87746-2_122.
Der volle Inhalt der QuelleSherman, David M. „5. Surface Complexation Modeling: Mineral Fluid Equilbria at the Molecular Scale“. In Thermodynamics and Kinetics of Water-Rock Interaction, herausgegeben von Eric H. Oelkers und Jacques Schott, 181–206. Berlin, Boston: De Gruyter, 2009. http://dx.doi.org/10.1515/9781501508462-007.
Der volle Inhalt der QuelleHöll, Wolfgang, Matthias Franzreb, Jürgen Horst und Siegfried Eberle. „Description of Ion-Exchange Equilibria by Means of the Surface Complexation Theory“. In Ion Exchange and Solvent Extraction, 151–209. Taylor & Francis Group, 6000 Broken Sound Parkway NW, Suite 300, Boca Raton, FL 33487-2742: CRC Press, 2017. http://dx.doi.org/10.4324/9780203749753-4.
Der volle Inhalt der QuelleTurner, David R., Susan Knox, Francisco Penedo, John G. Titley, John Hamilton-Taylor, Michael Kelly und Geraint L. Williams. „Surface Complexation Modelling of Plutonium Adsorption on Sediments of the Esk Estuary, Cumbria“. In Radionuclides in the Study of Marine Processes, 165–74. Dordrecht: Springer Netherlands, 1991. http://dx.doi.org/10.1007/978-94-011-3686-0_18.
Der volle Inhalt der QuelleKonferenzberichte zum Thema "Modélisation de la complexation de surface"
Erzuah, S., I. Fjelde und A. V. Omekeh. „Wettability Estimation by Surface Complexation Simulations“. In 79th EAGE Conference and Exhibition 2017 - SPE EUROPEC. Netherlands: EAGE Publications BV, 2017. http://dx.doi.org/10.3997/2214-4609.201701626.
Der volle Inhalt der QuelleErzuah, Samuel, Ingebret Fjelde und Aruoture Voke Omekeh. „Wettability Estimation by Surface Complexation Simulations“. In SPE Europec featured at 79th EAGE Conference and Exhibition. Society of Petroleum Engineers, 2017. http://dx.doi.org/10.2118/185767-ms.
Der volle Inhalt der QuelleBrady, Patrick Vane, James L. Krumhansl und Paul E. Mariner. „Surface Complexation Modeling for Improved Oil Recovery“. In SPE Improved Oil Recovery Symposium. Society of Petroleum Engineers, 2012. http://dx.doi.org/10.2118/153744-ms.
Der volle Inhalt der QuelleAbu-alsaud, M., A. Al-Ghamdi, S. Ayirala und A. Al-Sofi. „Surface Complexation Modeling of SmartWater Synergy with EOR in Carbonates“. In IOR 2021. European Association of Geoscientists & Engineers, 2021. http://dx.doi.org/10.3997/2214-4609.202133066.
Der volle Inhalt der QuelleKabengi, Nadine, Anastasia Ilgen, James Kubicki und Michael Machesky. „The Role of Cation Solvation Thermodynamics in Surface Complexation Reactions“. In Goldschmidt2021. France: European Association of Geochemistry, 2021. http://dx.doi.org/10.7185/gold2021.6454.
Der volle Inhalt der QuelleLi, Xiaodong, Eini Puhakka und Marja Siitari-kaupii. „Sorption of selenium species onto kaolinite surface: experiments, surface complexation modelling and DFT studies“. In Goldschmidt2021. France: European Association of Geochemistry, 2021. http://dx.doi.org/10.7185/gold2021.4677.
Der volle Inhalt der QuelleBompoti, N., M. Chrysochoou und M. Machesky. „Advances in Surface Complexation Modeling for Chromium Adsorption on Iron Oxide“. In Geo-Chicago 2016. Reston, VA: American Society of Civil Engineers, 2016. http://dx.doi.org/10.1061/9780784480168.001.
Der volle Inhalt der QuelleGustafsson, Jon Petter, Carin Sjöstedt und Charlotta Tiberg. „Using X-ray spectroscopic results to constrain surface complexation models: ferrihydrite“. In Goldschmidt2021. France: European Association of Geochemistry, 2021. http://dx.doi.org/10.7185/gold2021.6795.
Der volle Inhalt der QuelleElakneswaran, Y., M. Shimokawara, T. Nawa und S. Takahashi. „Surface Complexation and Equilibrium Modelling for Low Salinity Waterflooding in Sandstone Reservoirs“. In Abu Dhabi International Petroleum Exhibition & Conference. Society of Petroleum Engineers, 2017. http://dx.doi.org/10.2118/188621-ms.
Der volle Inhalt der QuelleAlessi, Daniel S., Md Samrat Alam, Janice P. L. Kenney und Kurt O. Konhauser. „UNDERSTANDING BIOCHAR-METAL INTERACTIONS USING COMBINED SPECTROSCOPIC AND SURFACE COMPLEXATION MODELLING APPROACHES“. In GSA Connects 2022 meeting in Denver, Colorado. Geological Society of America, 2022. http://dx.doi.org/10.1130/abs/2022am-382979.
Der volle Inhalt der QuelleBerichte der Organisationen zum Thema "Modélisation de la complexation de surface"
Sverjensky, Dimitri A. Predictive Surface Complexation Modeling. Office of Scientific and Technical Information (OSTI), November 2016. http://dx.doi.org/10.2172/1333692.
Der volle Inhalt der QuelleHayes, K., G. Redden, W. Ela und J. Leckie. Application of surface complexation models for radionuclide adsorption. Office of Scientific and Technical Information (OSTI), April 1990. http://dx.doi.org/10.2172/6914983.
Der volle Inhalt der QuelleHeinz, M. Review of "ML for Surface Complexation Model Development". Office of Scientific and Technical Information (OSTI), August 2020. http://dx.doi.org/10.2172/1670546.
Der volle Inhalt der QuelleZouabe, J., M. Zavarin und H. Wainwright. Machine Learning in Environmental Chemistry: Application to Surface Complexation Modeling. Office of Scientific and Technical Information (OSTI), September 2020. http://dx.doi.org/10.2172/1669226.
Der volle Inhalt der QuelleZavarin, M., J. Zouabe, E. Chang und H. Wainwright. M4SF-21LL010301062 Rev0 Non-Electrostatic Surface Complexation Database for GDSA. Office of Scientific and Technical Information (OSTI), Juli 2021. http://dx.doi.org/10.2172/1820018.
Der volle Inhalt der QuelleJ.L. Jerden Jr., A.J. Kropf und Y. Tsai. SURFACE COMPLEXATION OF ACTINIDES WITH IRON OXIDES: IMPLICATIONS FOR RADIONUCLIDE TRANSPORT IN NEAR-SURFACE AQUIFERS. Office of Scientific and Technical Information (OSTI), August 2005. http://dx.doi.org/10.2172/859262.
Der volle Inhalt der QuelleZavarin, M., E. Chang, S. Han und H. Wainwright. M4SF-22LL010301062-Surface Complexation Database and Hybrid ML Model Development for GDSA. Office of Scientific and Technical Information (OSTI), August 2022. http://dx.doi.org/10.2172/1880930.
Der volle Inhalt der QuelleZavarin, M. M4SF-19LL010301082-Surface Complexation and Ion Exchange Database Development Phase 1: Clay Minerals. Office of Scientific and Technical Information (OSTI), Juni 2019. http://dx.doi.org/10.2172/1529826.
Der volle Inhalt der QuellePowell, B., A. Kersting, M. Zavarin und P. Zhao. Development of a Composite Non-Electrostatic Surface Complexation Model Describing Plutonium Sorption to Aluminosilicates. Office of Scientific and Technical Information (OSTI), Oktober 2008. http://dx.doi.org/10.2172/1019063.
Der volle Inhalt der QuelleZavarin, M., E. Chang, S. Han und H. Wainwright. M4SF-23LL010301062-Surface Complexation/Ion Exchange Hybrid Model for Radionuclide Sorption to Clay Minerals. Office of Scientific and Technical Information (OSTI), Juli 2023. http://dx.doi.org/10.2172/1994028.
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