Bibliografías temáticas / Modélisation de la complexation de surface

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Literatura académica sobre el tema "Modélisation de la complexation de surface"

Autor: Grafiati
Publicado: 25 de mayo de 2024
Última modificación: 31 de julio de 2025

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Artículos de revistas sobre el tema "Modélisation de la complexation de surface"

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Katz, Lynn E., and Kim F. Hayes. "Surface Complexation Modeling." Journal of Colloid and Interface Science 170, no. 2 (1995): 477–90. http://dx.doi.org/10.1006/jcis.1995.1127.

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Katz, Lynn E., and Kim F. Hayes. "Surface Complexation Modeling." Journal of Colloid and Interface Science 170, no. 2 (1995): 491–501. http://dx.doi.org/10.1006/jcis.1995.1128.

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Ludwig, Christian, and Paul W. Schindler. "Surface Complexation on TiO2." Journal of Colloid and Interface Science 169, no. 2 (1995): 284–90. http://dx.doi.org/10.1006/jcis.1995.1035.

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Ludwig, Christian, and Paul W. Schindler. "Surface Complexation on TiO2." Journal of Colloid and Interface Science 169, no. 2 (1995): 291–99. http://dx.doi.org/10.1006/jcis.1995.1036.

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Dyrssen, David. "Sulfide complexation in surface seawater." Marine Chemistry 24, no. 2 (1988): 143–53. http://dx.doi.org/10.1016/0304-4203(88)90045-x.

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Forsling, Willis, and Liuming Wu. "Surface complexation at hydrous fluorapatite." Aquatic Sciences 55, no. 4 (1993): 336–46. http://dx.doi.org/10.1007/bf00877278.

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Belhamri, Azeddine, and 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, no. 1 (1998): 29–35. http://dx.doi.org/10.54966/jreen.v1i1.941.

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Il s'agit d'étudier le séchage de milieux poreux, particulièrement le comportement de la surface. Une analyse détaillée, de résultats d'expériences et leurs influences sur la modélisation, est présentée. Les moyens de mesures sont, principalement, une balance électronique, un pyromètre à infrarouge et un analyseur optique d'humidité de surface. Les évolutions de la température et de l'humidité de surface sont obtenues en fonction de la cinétique de séchage. Les résultats permettent, surtout, de caractériser le passage entre la première et la deuxième phase de séchage. Ils permettent, aussi, de
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Yao, Marcel Konan, Djedro Clément Akmel, Kouamé Lazare Akpetou, Albert Trokourey, Kouassi Benjamin Yao, and Nogbou Emmanuel Assidjo. "Modélisation de l'évolution spatiotemporelle du phosphore minéral dans une baie lagunaire hypereutrophe tropicale : la baie lagunaire de Tiagba (Côte d'Ivoire)." Revue des sciences de l’eau 30, no. 3 (2018): 247–58. http://dx.doi.org/10.7202/1044250ar.

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Ce travail décrit une nouvelle approche de la prédiction de l'évolution spatio-temporelle du phosphore minéral dans les eaux de surface, particulièrement dans la baie lagunaire de Tiagba. L'originalité de cette étude réside dans l'utilisation des réseaux de neurones artificiels, précisément du perceptron multicouche, comme outil de modélisation. Deux approches de l'évolution spatio-temporelle de ce nutriment dans cette baie ont été étudiées : sa modélisation statique et sa modélisation dynamique. Ainsi, il a été utilisé deux bases de 3 966 et 4 627 données respectivement pour sa modélisation s
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Erzuah, Samuel, Ingebret Fjelde, and Aruoture V. Omekeh. "Wettability Estimation Using Surface-Complexation Simulations." SPE Reservoir Evaluation & Engineering 22, no. 02 (2019): 509–19. http://dx.doi.org/10.2118/185767-pa.

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Traina, S. J. "Surface complexation modeling: Hydrous ferric oxide." Geochimica et Cosmochimica Acta 60, no. 21 (1996): 4291. http://dx.doi.org/10.1016/s0016-7037(97)81467-6.

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Tesis sobre el tema "Modélisation de la complexation de surface"

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Devau, Nicolas. "Processus rhizosphériques déterminant la disponibilité en phosphore : apport de la modélisation mécaniste géochimique." Thesis, Montpellier, SupAgro, 2010. http://www.theses.fr/2010NSAM0019.

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Les processus rhizosphériques sont reconnus comme une des stratégies majeures élaborées par les plantes afin d'augmenter la disponibilité en phosphore (P) et ainsi améliorer leur nutrition phosphatée. Pourtant, l'effet exact de ces processus est encore mal caractérisé et quantifié. L'objectif de ces travaux a été d e déterminer le rôle exercé par les modifications chimiques induites par les racines, particulièrement la modification de pH, dans les changements de disponibilité en P dans la rhizosphère. Pour ce faire, nous avons utilisé des modèles mécanistes géochimiques (« triple plane », écha
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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.

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Le principe du stockage en milieu géologique profond est de confiner les colis de déchets par un ensemble de barrières ouvragée et géologique. Les eaux souterraines constituent l'un des principaux points faibles de la sûreté d'un stockage en contribuant à l'altération des barrières et à la migration des radionucléides à travers la géosphère. Ainsi, la compréhension des processus susceptibles de retarder cette migration est fondamentale pour évaluer la sûreté d'un stockage. Le but de nos travaux est d'étudier les processus de sorption entre des phases de sulfures métalliques, présentes sous for
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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.

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L'objectif de cette étude est d'évaluer l'effet d'une augmentation de température sur les propriétés d'adsorption des minéraux argileux. La sorption et la désorption de Cs+, Ni2+ et Ln3+ sur une montmorillonite et une kaolinite ont été étudiées par des expériences " batch ", de 25 à 150°C, et dans différentes conditions de pH et de forces ioniques. Des enthalpies de sorption comprises entre 0 et 80kJ/mol environ ont ainsi été calculées. Pour l'europium, des analyses spectroscopiques de surface ont confirmé que le mécanisme impliqué était bien un mécanisme d'adsorption, y compris à 150°C. De pl
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Gao, Pengyuan. "Theoretical Studies of the Interaction between U(VI) and Mineral Surfaces." Electronic Thesis or Diss., Orléans, 2023. http://www.theses.fr/2023ORLE1074.

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L'étude des processus d'adsorption des radionucléides sur les surfaces minérales est fondamentale pour la conception et l'évaluation de la sûreté des futurs systèmes de stockage des déchets radioactifs, ainsi que pour les diagnostics environnementaux des milieux pollués par des radionucléides. Parmi ces radionucléides, l'uranium a une abondance relativement élevée dans les systèmes naturels et a un rôle central dans le cycle du combustible nucléaire. L’uranium peut se trouver sous plusieurs états d’oxydation. L'U(VI) est l'état d'oxydation le plus pertinent dans la plupart des eaux de surface
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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.

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Les minéraux argileux sont omniprésents dans les environnements géologiques de surface et sub-surface du globe terrestre. Parmi eux, ceux qu'on appelle communément " argiles gonflantes " peuvent être de très petite taille (<2µm) et de fait adsorber de grandes quantités d'eau et de solutés à leurs surfaces. De ce fait, même en faible proportion, les minéraux argileux gonflants peuvent contrôler une grande partie des propriétés physiques, mécaniques et chimiques des environnements dans lesquels ils sont présents. Ce manuscrit se focalise sur différents modèles, basés sur des formalismes thermody
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Bengtsson, 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.

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Apatites are a diverse class of phosphate minerals that are important in a great variety of natural and industrial processes. They are, for example, used as raw material in fertiliser production and in the remediation of metal-contaminated soils. Hydroxyapatite Ca5(PO4)3OH, (HAP) and fluorapatite Ca5(PO4)3F, (FAP) are similar to the biological apatite that is the main constituent of mammalian bone and teeth, and they are therefore promising materials for artificial bone and tooth implants. This thesis is a summary of four papers with focus on dissolution and surface complexation reactions of H
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Bengtsson, 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.

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Wu, Liuming. "Surface complexation at calcium mineral-water interfaces." Doctoral thesis, Luleå, 1994. http://urn.kb.se/resolve?urn=urn:nbn:se:ltu:diva-25727.

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Surface reactions occurring at solid-water interfaces in calcium mineral-ligands systems have been studied. Both hydrous apatite and fluorite surfaces show clear amphoteric properties. An ion exchange process between lattice ions of F- on fluorite and OH- ions in bulk solution is discovered. The surface adsorption of Alizarin Red S and sodium oleate are determined. Surface chemical reaction models are established based on acidbase potentiometric titrations, solubility, adsorption and zeta-potential measurements in 0. 1 mol dm-3 ionic media at 25'C. Experimental data are evaluated using the com
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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.

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The adsorption behaviour of trace metals in soil may provide us with a way to more accurately predict and assess the toxicity of metals in the environment. This thesis reports efforts to apply surface complexation modeling to agricultural and forest soil and to relate model parameters to common soil properties. This study considered Ca, Cd, Cu, Pb and Zn but the methods here could be applied to other metals. In Chapter 2, the surface charge and adsorption behaviour of a set of Ap horizons was characterised using back-titration and batch adsorption techniques. With the objective of simpl
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Gisler, 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.

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Libros sobre el tema "Modélisation de la complexation de surface"

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Karamalidis, Athanasios K., and David A. Dzombak. Surface Complexation Modeling. John Wiley & Sons, Inc., 2010. http://dx.doi.org/10.1002/9780470642665.

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Johannes, Lützenkirchen, ed. Surface complexation modelling. Elsevier/Academic Press, 2006.

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A, Dzombak David, ed. Surface complexation modeling: Gibbsite. Wiley, 2010.

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Dzombak, David A. Surface complexation modeling: Hydrous ferric oxide. Wiley, 1990.

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Harvey, K. B. Surface-complexation models for sorption onto heterogeneous surfaces. Whiteshell Laboratories, 1997.

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B, 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., and Sandia National Laboratories, eds. Surface-complexation modeling of radionuclide adsorption in subsurface environments. Division of High-Level Waste Management, Office of Nuclear Material Safety and Safeguards, U.S. Nuclear Regulatory Commission, 1988.

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B, 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., and Sandia National Laboratories, eds. Surface-complexation modeling of radionuclide adsorption in subsurface environments. Division of High-Level Waste Management, Office of Nuclear Material Safety and Safeguards, U.S. Nuclear Regulatory Commission, 1988.

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1953-, Hayes Kim F., U.S. Nuclear Regulatory Commission. Division of Low-Level Waste Management and Decommissioning., and Stanford University. Dept. of Civil Engineering., eds. Application of surface complexation models for radionuclide adsorption: Sensitivity analysis of model input parameters. Division of Low-Level Waste Management and Decommissioning, Office of Nuclear Material Safety and Safeguards, U.S. Nuclear Regulatory Commission, 1990.

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1953-, Hayes Kim F., U.S. Nuclear Regulatory Commission. Division of Low-Level Waste Management and Decommissioning., and Stanford University. Dept. of Civil Engineering., eds. Application of surface complexation models for radionuclide adsorption: Sensitivity analysis of model input parameters. Division of Low-Level Waste Management and Decommissioning, Office of Nuclear Material Safety and Safeguards, U.S. Nuclear Regulatory Commission, 1990.

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Su, Pu-chʻing. Computational geometry--curve and surface modeling. Academic Press, 1989.

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Capítulos de libros sobre el tema "Modélisation de la complexation de surface"

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Sun, Z. X., and W. Forsling. "Mineral Surface Complexation in Flotation." In Innovations in Flotation Technology. Springer Netherlands, 1992. http://dx.doi.org/10.1007/978-94-011-2658-8_11.

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Anderson, Paul R., and Mark M. Benjamin. "Constant-Capacitance Surface Complexation Model." In ACS Symposium Series. American Chemical Society, 1990. http://dx.doi.org/10.1021/bk-1990-0416.ch021.

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Schindler, P. W., and G. Sposito. "Surface Complexation at (Hydr)Oxide Surfaces." In Interactions at the Soil Colloid — Soil Solution Interface. Springer Netherlands, 1991. http://dx.doi.org/10.1007/978-94-017-1909-4_4.

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Mu, Q. S., Y. H. Ma, A. L. Lewis, S. P. Armes, and J. R. Lu. "Complexation of DNA with biocompatible diblock copolymers." In Surface and Colloid Science. Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/b97072.

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Sposito, Garrison. "Surface Complexation of Metals by Natural Colloids." In Ion Exchange and Solvent Extraction. CRC Press, 2017. http://dx.doi.org/10.4324/9780203749753-5.

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Davis, J. A., and D. B. Kent. "CHAPTER 5. SURFACE COMPLEXATION MODELING IN AQUEOUS GEOCHEMISTRY." In Mineral-Water Interface Geochemistry, edited by Michael F. Hochella and Art F. White. De Gruyter, 1990. http://dx.doi.org/10.1515/9781501509131-009.

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Sherman, David M., Chris G. Hubbard, and Caroline L. Peacock. "Surface complexation of U(VI) by Fe and Mn (hydr)oxides." In Uranium, Mining and Hydrogeology. Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-87746-2_122.

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Sherman, David M. "5. Surface Complexation Modeling: Mineral Fluid Equilbria at the Molecular Scale." In Thermodynamics and Kinetics of Water-Rock Interaction, edited by Eric H. Oelkers and Jacques Schott. De Gruyter, 2009. http://dx.doi.org/10.1515/9781501508462-007.

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Höll, Wolfgang, Matthias Franzreb, Jürgen Horst, and Siegfried Eberle. "Description of Ion-Exchange Equilibria by Means of the Surface Complexation Theory." In Ion Exchange and Solvent Extraction. CRC Press, 2017. http://dx.doi.org/10.4324/9780203749753-4.

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Turner, David R., Susan Knox, Francisco Penedo, et al. "Surface Complexation Modelling of Plutonium Adsorption on Sediments of the Esk Estuary, Cumbria." In Radionuclides in the Study of Marine Processes. Springer Netherlands, 1991. http://dx.doi.org/10.1007/978-94-011-3686-0_18.

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Actas de conferencias sobre el tema "Modélisation de la complexation de surface"

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Yoffe, Pavel. "Complexation Influenced Corrosion at Thermal Power Plants." In CORROSION 2001. NACE International, 2001. https://doi.org/10.5006/c2001-01497.

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Abstract Hydrazine injection to feedwater is generally used for of steam deoxigination in IEC Power Plants (PP). This work is based on result of laboratory investigation that is performed during lust ten years, while schedul PP interrupting. In oxygen presence copper-ammonia complex (CAC) is generated. Transferred through the steam circle CAC dissociates and copper beads deposit on evaporator tube internal surface. A following idea that seems be enough versivilar. As condenser tube material as steel components are leached out of the metal due to metal-ammonia and metal-hydrazine complexation.
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Ferrer, Ana, Yolanda De-Abreu, and Carol Roach. "Evaluating the Impact of Different Families of Scale Inhibitors on Corrosion Inhibitor Performance by Surface Tension and Electrochemical Impedance Spectroscopy Measurements." In CORROSION 2018. NACE International, 2018. https://doi.org/10.5006/c2018-11505.

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Abstract It is well known that chemical interactions between scale inhibitor (SI) and corrosion inhibitor (CI) might lead to a reduction in the performance efficiency of both chemicals. Scale and corrosion inhibitors are widely used in the oil and gas industry; thus it is very important to understand how they impact each other's performance. This paper attempted to explain how different families of scale inhibitors impact corrosion inhibitors performance in the presence of each other. For this purpose, this paper addressed fundamental properties of both chemistries and how their interaction ca
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Natsi, P. D., E. Zande, and P. G. Koutsoukos. "Protective Coatings against Formation of Scale Deposits." In CONFERENCE 2023. AMPP, 2023. https://doi.org/10.5006/c2023-19528.

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Abstract Hydrophilic polymers are known to induce the deposition of sparingly soluble salts. Poly-2-hydroxyethyl methacrylate, (PHEMA), a hydrogel used for the fabrication of contact and intraocular lenses has been reported to favor the nucleation and crystal growth of calcium phosphate. PHEMA disks coated with graphene oxide (GO) were good nucleators of Hydroxyapatite (HAP). which precipitated at rates higher in comparison with the respective on the uncoated material. The mechanism of HAP crystal growth was controlled by surface diffusion as shown by the dependence of the rates on the relativ
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King, Fraser, Miroslav Kolář, and David W. Shoesmith. "Modelling the Effects of Porous and Semi-Permeable Layers on Corrosion Processes." In CORROSION 1996. NACE International, 1996. https://doi.org/10.5006/c1996-96380.

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Abstract Porous and semi-permeable layers play a role in many corrosion processes. Porous layers may simply affect the rate of corrosion by affecting the rate of mass transport of reactants and products to and from the corroding surface. Semi-permeable layers can further affect the corrosion process by reacting with products and/or reactants. Reactions in semi-permeable layers include redox processes involving electron transfer, adsorption, ion-exchange and complexation reactions and precipitation/dissolution processes. Examples of porous and semi-permeable layers include non-reactive salt fil
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Koutsoukos, Petros G., and Aikaterini N. Kofina. "Struvite Scale Formation and Inhibition in Wastewater." In CORROSION 2007. NACE International, 2007. https://doi.org/10.5006/c2007-07057.

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Abstract The formation of struvite scale formation was investigated in synthetic wastewater, 25°C, pH 8.50 both in the absence and in the presence of heavy metals cadmium(Cd), copper (Cu) and lead (Pb). The concentrations of the tested metals was in the range between 1-10 μM to avoid metal hydroxide precipitation. The investigation was done at conditions of constant supersaturation. Synthetic wastewater, aqueous solutions with composition similar to typical municipal wastewater was used as a matrix for the preparation of the supersaturated solutions. The kinetics of struvite precipitation was
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Koutsoukos, Petros G., P. Klepetsanis, N. Spanos, and D. G. Kanellopoulou. "Calcium Carbonate Crystal Growth and Dissolution Inhibitors." In CORROSION 2007. NACE International, 2007. https://doi.org/10.5006/c2007-07052.

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Abstract Calcium carbonate scale formation was simulated by the development in situ of supersaturation in the vicinity of a stainless steel electrode immersed in a stable calcium carbonate solution. The initiation of the growth of the supercritical crystals was accompanied by a decrease of the absolute value of the cathodic current, which at the end of crystallization was constant. The absolute final value of the cathodic current was the measure of the extent of crystallization. In the absence of any additive the only phase identified on the electrode was calcite. In the presence however of ad
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Coutelot, Fanny, and Brian Powell. "Surface-mediated reduction in plutonium surface complexation modelling." In Goldschmidt 2024. Geochemical Society, 2024. https://doi.org/10.46427/gold2024.24608.

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Erzuah, S., I. Fjelde, and A. V. Omekeh. "Wettability Estimation by Surface Complexation Simulations." In 79th EAGE Conference and Exhibition 2017 - SPE EUROPEC. EAGE Publications BV, 2017. http://dx.doi.org/10.3997/2214-4609.201701626.

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Erzuah, Samuel, Ingebret Fjelde, and 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.

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Brady, Patrick Vane, James L. Krumhansl, and 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.

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Informes sobre el tema "Modélisation de la complexation de surface"

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Sverjensky, Dimitri A. Predictive Surface Complexation Modeling. Office of Scientific and Technical Information (OSTI), 2016. http://dx.doi.org/10.2172/1333692.

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Hayes, K., G. Redden, W. Ela, and J. Leckie. Application of surface complexation models for radionuclide adsorption. Office of Scientific and Technical Information (OSTI), 1990. http://dx.doi.org/10.2172/6914983.

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Heinz, M. Review of "ML for Surface Complexation Model Development". Office of Scientific and Technical Information (OSTI), 2020. http://dx.doi.org/10.2172/1670546.

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Zouabe, J., M. Zavarin, and H. Wainwright. Machine Learning in Environmental Chemistry: Application to Surface Complexation Modeling. Office of Scientific and Technical Information (OSTI), 2020. http://dx.doi.org/10.2172/1669226.

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Zavarin, M., J. Zouabe, E. Chang, and H. Wainwright. M4SF-21LL010301062 Rev0 Non-Electrostatic Surface Complexation Database for GDSA. Office of Scientific and Technical Information (OSTI), 2021. http://dx.doi.org/10.2172/1820018.

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J.L. Jerden Jr., A.J. Kropf, and Y. Tsai. SURFACE COMPLEXATION OF ACTINIDES WITH IRON OXIDES: IMPLICATIONS FOR RADIONUCLIDE TRANSPORT IN NEAR-SURFACE AQUIFERS. Office of Scientific and Technical Information (OSTI), 2005. http://dx.doi.org/10.2172/859262.

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Zavarin, M., E. Chang, S. Han, and H. Wainwright. M4SF-22LL010301062-Surface Complexation Database and Hybrid ML Model Development for GDSA. Office of Scientific and Technical Information (OSTI), 2022. http://dx.doi.org/10.2172/1880930.

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Zavarin, M. M4SF-19LL010301082-Surface Complexation and Ion Exchange Database Development Phase 1: Clay Minerals. Office of Scientific and Technical Information (OSTI), 2019. http://dx.doi.org/10.2172/1529826.

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Powell, B., A. Kersting, M. Zavarin, and P. Zhao. Development of a Composite Non-Electrostatic Surface Complexation Model Describing Plutonium Sorption to Aluminosilicates. Office of Scientific and Technical Information (OSTI), 2008. http://dx.doi.org/10.2172/1019063.

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Zavarin, M., E. Chang, S. Han, and H. Wainwright. M4SF-23LL010301062-Surface Complexation/Ion Exchange Hybrid Model for Radionuclide Sorption to Clay Minerals. Office of Scientific and Technical Information (OSTI), 2023. http://dx.doi.org/10.2172/1994028.

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