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Relevant bibliographies by topics / Adsorption des cations

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Academic literature on the topic 'Adsorption des cations'

Author: Grafiati

Published: 4 June 2021

Last updated: 6 February 2022

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Journal articles on the topic "Adsorption des cations"

1

Noor, Ehteram A., and Fatma M. Al-Solmi. "Analysis of Adsorption, Ion Exchange, Thermodynamic Behaviour of Some Organic Cations on Dowex 50WX4-50/H+Cation Exchanger in Aqueous Solutions." E-Journal of Chemistry 8, s1 (2011): S171—S188. http://dx.doi.org/10.1155/2011/963603.

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The equilibrium adsorption, ion exchange characteristics of various concentrations of some organic cations from aqueous solutions onto dowex 50WEX/H+cation exchanger were studied at different temperatures in the range of 30-50 °C. The studied cations showed good adsorptive properties onto dowex 50WX4-5/H+at different concentrations and temperatures. Main adsorption behaviour was ion exchange between hydrogen ions and the organic cations as indicated from the linear relation between the initial concentration of the organic cations and the released hydrogen ions. It was found that the adsorption

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2

Patrício, Aline Cadigena Lima, Marcílio Máximo da Silva, Anna Karoline Freires de Sousa, Mariaugusta Ferreira Mota, and Meiry Glaúcia Freire Rodrigues. "SEM, XRF, XRD, Nitrogen Adsorption, Fosters Swelling and Capacity Adsorption Characterization of Cloisite 30 B." Materials Science Forum 727-728 (August 2012): 1591–95. http://dx.doi.org/10.4028/www.scientific.net/msf.727-728.1591.

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Cationic surfactants, such as quaternary ammonium cations, have been used, in order to ameliorate the oil sorption capacity of inorganics materials, such as clays. Clays modified with quaternary ammonium cations (organoclays) have better performance in sorption, remove oil and grease from water at seven times the rate of activated carbon, as well as they can be used like perforation fluids of oil wells to the oil base, lubricants, among others industries. This work aims characterize the Cloisite 30B using various techniques: X-Ray Diffraction (XRD), Specific Surface Area (BET) and Cation Excha

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Schramm, Laurier L., Shmuel Yariv, Dipak K. Ghosh, and Loren G. Hepler. "Electrokinetic study of the adsorption of ethyl violet and crystal violet by montmorillonite clay particles." Canadian Journal of Chemistry 75, no. 12 (1997): 1868–77. http://dx.doi.org/10.1139/v97-620.

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Electrophoretic mobilities of mixtures of a montmorillonite clay (in different exchangeable metal cation forms) and increasing amounts of two cationic dyes (ethyl violet and crystal violet) were measured. Electrophoretic mobilities were found to vary between −60 × 10−5 and +40 × 10−5 cm2 s−1 V−1. For both the dyes, the degree of saturation at which the isoelectric point (IEP) occurs, decreases with increasing valency of the metal cations. An effort was made to connect the IEP, maximum flocculation, and dye adsorption parameters. An important adsorption parameter is the transition saturation (T

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Wang, Shiyu, Junnan Zhang, Fada Zhou, et al. "Adsorption of EDCs on Reclaimed Water-Irrigated Soils: A Comparative Analysis of a Branched Nonylphenol, Nonylphenol and Bisphenol A." Water 13, no. 18 (2021): 2532. http://dx.doi.org/10.3390/w13182532.

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Nonylphenol (NP) and bisphenol A (BPA) are two typical endocrine disrupter chemicals (EDCs) in reclaimed water. In this study, the adsorptions of NP, a branched NP (NP7) and BPA on reclaimed water-irrigated soils were studied by isothermal experiments, and the different environmental factors on their adsorptions were investigated. The results showed that the adsorptions of NP and NP7 on soils conformed to the Linear model, and the adsorption of BPA conformed to the Freundlich model. The adsorptions of NP, NP7 and BPA on soils decreased with increasing temperatures and pHs. Adsorption equilibri

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Morillo, E., J. L. Pérez-Rodríguez, and C. Maqueda. "Mechanisms of interaction between montmorillonite and 3-aminotriazole." Clay Minerals 26, no. 2 (1991): 269–79. http://dx.doi.org/10.1180/claymin.1991.026.2.10.

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AbstractThe adsorption of aminotriazole, at its solution pH, with montmorillonite saturated with different cations has been studied. A pesticide-montmorillonite complex is formed through interlamellar cations which are not displaced. Aminotriazole is situated mostly as a polarized molecule around Mg2+ and Zn2+ cations, removing a great amount of water. In Na+- and Li+-montmorillonite, the pesticide remains as a non-polarized molecule, hydration water being retained in the interlamellar space; the pesticide is coordinated to interlamellar cations through water bridges. For all samples a proport

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Carotenuto, Gianfranco. "Isothermal Kinetic Investigation of the Water-Cations Interaction in Natural Clinoptilolite." European Journal of Engineering Research and Science 4, no. 5 (2019): 119–25. http://dx.doi.org/10.24018/ejers.2019.4.5.1341.

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The kinetics of water adsorption by a natural zeolite (clinoptilolite) sample has been investigated by high-frequency AC current intensity measurements. According to the achieved kinetic results, cations should play a relevant role in the clinoptilolite hydration, in fact most of adsorbed water stay in the cationic sites. The water molecules associate withcation one-by-one. In particular, the forced adsorption of water molecules in a wet atmosphere is a quite slow process, while water desorption in air or dry atmosphere is a spontaneous and fast process. The observed increase of cation mobilit

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Seo, Ji Hae, Namgyu Kim, Munsik Park, Sunkyung Lee, Seungjae Yeon, and Donghee Park. "Evaluation of metal removal performance of rod-type biosorbent prepared from sewage-sludge." Environmental Engineering Research 25, no. 5 (2019): 700–706. http://dx.doi.org/10.4491/eer.2019.201.

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The aim of this work was to evaluate the potential use of recycled sewage-sludge as a biosorbent for removing various metals from aqueous solution. To improve adsorption capacity and accomplish easy solid-liquid separation, the sludge was immobilized into the rod type with Ca-alginate. The removal performance was analyzed through kinetic and equilibrium studies. We conducted batch experiments examining the removal of cationic metals and anionic metals/metalloid by the rod-type biosorbent (cations: Cd(II), Cu(II), Cr(III), Fe(II), Ni(II), Pb(II), Zn(II), Mn(II), Al(III), As(III), and Fe(III); a

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Maqueda, C., and E. Morillo. "Sorption of chlormequat on montmorillonite as affected by dissolved copper. Influence of background electrolytes." Clay Minerals 36, no. 4 (2001): 473–81. http://dx.doi.org/10.1180/0009855013640002.

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AbstractIn this paper, the role of Cu in the adsorption of the cationic pesticide chlormequat (CCC) on montmorillonite is studied. The adsorption of CCC was measured in various media, e.g. water and aqueous solutions of NaCl, CaCl2 and Ca(NO3)2 at the same ionic strength (I= 0.01 mol l–1). The retention of CCC on montmorillonite in aqueous media is due principally to a cationic exchange process with inorganic cations which saturate the interlamellar positions on this mineral. However, the amount of inorganic cations liberated from montmorillonite was ∼15% less than the amount of CCC adsorbed.

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Tahraoui, Zakaria, Habiba Nouali, Claire Marichal, Patrice Forler, Julien Klein, and T. Jean Daou. "Influence of the Compensating Cation Nature on the Water Adsorption Properties of Zeolites." Molecules 25, no. 4 (2020): 944. http://dx.doi.org/10.3390/molecules25040944.

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The influence of the compensating cation (Na+, Li+, Mg2+) nature on the water adsorption properties of LTA and FAU-type zeolites was investigated. Cation exchanges were performed at 80 °C for 2 h using 1 M aqueous solutions of lithium chloride (LiCl) or magnesium chloride (MgCl2). XRF and ICP-OES analyses indicate that the cation exchange yields reach values between 59 to 89% depending on the number of exchange cycles and the nature of the zeolite and cation, while both zeolites structures are preserved during the process, as shown by XRD and solid state NMR analyses. Nitrogen adsorption-desor

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Sun, Wei-Feng, Yu-Xuan Sun, Shu-Ting Zhang, and Ming-He Chi. "Hydrogen Storage, Magnetism and Electrochromism of Silver Doped FAU Zeolite: First-principles Calculations and Molecular Simulations." Polymers 11, no. 2 (2019): 279. http://dx.doi.org/10.3390/polym11020279.

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The complex configuration, H2 adsorption binding energy, magnetic, and optical properties of FAU zeolites with Ag cations loaded by ion exchange in the vacant dielectric cavities were investigated by employing the first-principles calculations with all-electron-relativistic numerical atom-orbitals scheme and the Metropolis Monte Carlo molecular simulations. The visible absorption spectrum peaked at distinct wavelengths arranging from red or green to blue colors when changing the net charge load, due to the produced various redox states of Ag cations exchanging at multiple Li+-substituted sites

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Dissertations / Theses on the topic "Adsorption des cations"

1

Hocine, Sarah. "Adsorption des cations alcalins et phénomènes électrocinétiques sur les surfaces de silices chargéess." Thesis, Montpellier, 2017. http://www.theses.fr/2017MONTT193/document.

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Dans les structures confinées, comme les silices mésoporeuses, la mobilité et l'interaction des cations avec les surfaces sont des phénomènes clés. Ils guident les propriétés d'adsorption dont découlent de nombreuses applications, en particulier pour l’extraction et la séparation. Ce travail de thèse en modélisation propose de s'intéresser aux propriétés d'interface, d'équilibre et de transport qui pilotent l'échange ou l'adsorption ionique. Il s’agit de décrire la physico-chimie du processus d’adsorption de cations alcalins à la surface de silices chargée par une approche multiéchelle ayant u

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Leclerc, Véronique. "Etude de la coadsorption de molécules organiques et de cations minéraux sur charbons actifs." Limoges, 1995. http://www.theses.fr/1995LIMO0017.

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Ce travail a pour objet l'etude de la coadsorption sur differents charbons actifs en poudre (cap), de molecules organiques, l'atrazine et le diuron en presence d'un tensioactif anionique, le dodecylsulfate de sodium, avec ou sans cations divalents. On montre dans ce travail: que les herbicides et le tensioactif seuls s'adsorbent en fonction de la surface specifique et des fonctions de surface des charbons. Ainsi on peut classer les cap selon l'ordre croissant de leur capacite maximale d'adsorption: ceca, picazine, chemviron f 400. Que les cations presents majoritairement a la surface des charb

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3

Pamar-Robert, Arlette. "L'Adsorption en phase liquide, moyen d'étude de l'insertion des composés organiques dans la montmorillonite." Toulouse, INPT, 1991. http://www.theses.fr/1991INPT032G.

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La formation et la structure des complexes d'insertion argilo-organiques peuvent etre etudiees a partir des isothermes d'adsorption en phase liquide. Avec les montmorillonites echangees par divers cations (mg, ca, na, k), les isothermes d'adsorption composites de melanges binaires de composes organiques polaires avec le benzene montrent que le benzene est exclu de l'insertion. A partir des quantites inserees, deduites des isothermes, il est possible de calculer l'aire d'encombrement des molecules polaires inserees et d'en deduire leur orientation entre les feuillets. Avec les montmorillonites

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4

Buttefey, Séverine. "Modélisation et simulation moléculaire des cations extra-charpentes dans les zéolithes de type faujasite : effet du nombre et de la localisation des cations sur les phénomènes d'adsorption." Paris 11, 2002. http://www.theses.fr/2002PA112104.

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L'étude par simulation moléculaire de l'adsorption d'eau et des isomères du xylène dans les zéolithes de type faujasite a été réalisée dans le but de comprendre comment la présence d'une faible quantité d'eau dans la zéolithe peut modifier la sélectivité en faveur de l'un ou l'autre des isomères. Dans la première partie de ce travail, un modèle simple de distribution cationique dans les sites cristallographiques I, I', II et III a été proposé dans les zéolithes NaY et NaX. Ce modèle est basé sur le fait que la distribution cationique est induite par la répulsion électrostatique entre cations.

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5

Khabzina, Yoldes. "Influence des cations d'échange dans les zéolithes type faujasites sur la sélectivité d'adsorption des isomères du xylène." Thesis, Lyon 1, 2015. http://www.theses.fr/2015LYO10008.

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Depuis plusieurs années, IFPEN développe des adsorbants à base de zéolithe faujasite pour le procédé de séparation des xylènes. Dans ce cadre, cette thèse a permis de rationaliser les origines de la sélectivité des isomères du xylène dans les zéolithes faujasites. Pour ce faire, une nouvelle approche est proposée. L'objectif est d'établir un modèle à la fois explicatif et prédictif qui permet de relier la sélectivité à un certain nombre de paramètres caractéristiques du système, appelés descripteurs. Après la proposition d'un plan d'expériences contenant une soixantaine d'adsorbants, leur prép

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6

Coasne, Benoit, Guillaume Maurin, Anne Nicolas, Sabine Devautour-Vinot, Jean-Charles Giuntini, and François Henn. "Effect of water adsorption on the thermodynamics and dynamics of the extra-framework cations in zeolite systems: Effect of water adsorption on the thermodynamics and dynamics ofthe extra-framework cations in zeolite systems." Diffusion fundamentals 2 (2005) 13, S. 1-2, 2005. https://ul.qucosa.de/id/qucosa%3A14342.

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7

Bardot, Frédérique. "Les minéraux argileux et leur hétérogénéité superficielle : influence de la nature des cations compensateurs superficiels de l'illite sur les mécanismes d'adsorption de gaz." Vandoeuvre-les-Nancy, INPL, 1998. http://docnum.univ-lorraine.fr/public/INPL_T_1998_BARDOT_F.pdf.

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Cette étude contribue à la compréhension des mécanismes d'adsorption de gaz à la surface des minéraux argileux. Le solide utilise est un phyllosilicate 2:1, l'illite du puy. Après purification, neufs échantillons ont été préparés en échangeant les cations compensateurs superficiels avec Li+,Na+, K+, Rb+, Cs+, Mg²+, Ca²+, Sr²+ ou Ba²+. Ces échantillons ont fait l'objet d'une caractérisation préalable par analyses chimiques, thermiques et texturales. Les résultats obtenus montrent que les particules élémentaires sont formées de 5 à 6 feuillets, de surface spécifique de l'ordre de 170 m²/g et org

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Coasne, Benoit, Guillaume Maurin, Anne Nicolas, Sabine Devautour-Vinot, Jean-Charles Giuntini, and François Henn. "Effect of water adsorption on the thermodynamics and dynamics of the extra-framework cations in zeolite systems." Universitätsbibliothek Leipzig, 2016. http://nbn-resolving.de/urn:nbn:de:bsz:15-qucosa-195245.

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Bekhti, Widad. "Synthèse par voie hydrothermale et caractérisation des micro/nanostructures d’Oxyde de Zinc." Thesis, Lyon 1, 2015. http://www.theses.fr/2015LYO10015.

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L'oxyde de zinc (ZnO) est un matériau semi-conducteur qui présente des caractéristiques très intéressantes telles que : un gap directe à 3.3 eV à température ambiante, une forte énergie excitonique (60 meV à température ambiante) associé à un caractère piézoélectrique. Ces propriétés permettent de considérer le ZnO parmi les nanomatériaux prometteurs, dans une grande variété d'applications : dans le domaine de l'optoélectronique, de l'énergie photovoltaïque ou de l'environnement. Pour que ces dispositifs deviennent exploitables à l'échelle industrielle, certaines conditions doivent être satisf

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Melo, Junior Mauricio Alves de 1981. "Sintese de silica e filossilicatos organofuncionalizados : estudos de adsorção e termoquimica de interação com cations metalicos." [s.n.], 2008. http://repositorio.unicamp.br/jspui/handle/REPOSIP/250074.

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Orientador: Claudio Airoldi<br>Tese (doutorado) - Universidade Estadual de Campinas, Instituto de Quimica<br>Made available in DSpace on 2018-08-11T06:59:18Z (GMT). No. of bitstreams: 1 MeloJunior_MauricioAlvesde_D.pdf: 5727295 bytes, checksum: f6680a1dc4c1e8e3bcc70187b640db77 (MD5) Previous issue date: 2008<br>Resumo: Dois novos agentes sililantes foram sintetizados através das reações individuais das moléculas etanolamina e dietanolamina com o precursor 3- glicidoxidopropiltrimetoxissilano. Estas interações foram possíveis pela abertura do anel epóxido, presente na extremidade da cadeia do

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Books on the topic "Adsorption des cations"

1

Bobacka, Veronica. Interactions between cationic starch and components of a peroxide-bleached thermomechanical pulp. Åbo Academy Press, 2001.

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2

Lach, Joanna. Wpływ sposobu modyfikacji węgli aktywnych na adsorpcję metali ciężkich. Wydawn. Politechniki Częstochowskiej, 2011.

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Lawrence, Monique Ann Marie. The adsorption of phenolic and organotin compounds by clays and cation exchanged clays. Aston University. Department of Chemical Engineering and Applied Chemistry, 1996.

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Crow, Roger D. The influence of aluminum salts on the adsorption of cationic polyelectrolyte by cellulosic fibers. Institute of Paper Chemistry, 1985.

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5

Westall, John C. The use of cationic surfactants to modify aquifer materials to reduce the mobility of hydrophobic organic compounds / John C. Westall ... [et al.]. U.S. Environmental Protection Agency, Robert S. Kerr Environmental Research Laboratory, 1994.

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Westall, John C. The use of cationic surfactants to modify aquifer materials to reduce the mobility of hydrophobic organic compounds / John C. Westall ... [et al.]. U.S. Environmental Protection Agency, Robert S. Kerr Environmental Research Laboratory, 1994.

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Naraian, Prakash. Evaluation of a streaming current detector to measure cationic starch adsorption on papermaking fibers and fines. 1998.

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Book chapters on the topic "Adsorption des cations"

1

Rao, Feng, Zhili Li, and Ramiro Escudero Garcia. "Adsorption of Cations on Minerals." In Adsorption at Natural Minerals/Water Interfaces. Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-54451-5_5.

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Maurin, G., S. Devautour, P. Senet, J. C. Giuntini, and F. Henn. "Cations Mobility and Water Adsorption in Zeolites." In New Trends in Intercalation Compounds for Energy Storage. Springer Netherlands, 2002. http://dx.doi.org/10.1007/978-94-010-0389-6_25.

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Papachristou, E., G. Vasilikiotis, and C. Alexiades. "Selective Adsorption of Heavy Metal Cations by Using Fly Ash." In Appropriate Waste Management for Developing Countries. Springer US, 1985. http://dx.doi.org/10.1007/978-1-4613-2457-7_28.

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Ogrinc, N., I. Kobal, E. Matijević, and N. Kallay. "Adsorption of Cations on Colloidal Oxide Particles. Cobalt Ions on Hematite." In Fine Particles Science and Technology. Springer Netherlands, 1996. http://dx.doi.org/10.1007/978-94-009-0259-6_7.

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Świątkowski, Andrzej, Grzegorz Szymański, and Stanisław Biniak. "Adsorption from Aqueous Solutions of Selected Heavy Metal Cations on Chemically Modified Activated Carbon." In The Kluwer International Series in Engineering and Computer Science. Springer US, 1996. http://dx.doi.org/10.1007/978-1-4613-1375-5_114.

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Ha, Ki-Sung. "Gas Adsorption Characteristics of Cation-Exchanged Natural Zeolite." In The Kluwer International Series in Engineering and Computer Science. Springer US, 1996. http://dx.doi.org/10.1007/978-1-4613-1375-5_43.

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Devore, D. I., N. S. Clungeon, and S. A. Fischer. "Adsorption and Viscoelastic Properties of Thermosetting Cationic Polyelectrolytes." In ACS Symposium Series. American Chemical Society, 1993. http://dx.doi.org/10.1021/bk-1994-0548.ch030.

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Bakker, Martin G., Gregory L. Turner, John Matthews, and Kunliang Zhang. "Studies of Adsorption and Aggregation of Cationic Surfactants on Silica Surfaces Using EPR." In ACS Symposium Series. American Chemical Society, 1999. http://dx.doi.org/10.1021/bk-2000-0740.ch016.

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Gillespie, Christopher. "Utilizing mAb Adsorption Isotherms To Direct Process Development of a Strong Cation-Exchange Chromatography Step." In ACS Symposium Series. American Chemical Society, 2013. http://dx.doi.org/10.1021/bk-2013-1125.ch004.

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Hanna, John. "Adsorption and Wetting Characteristics of Pure Non-metallic Minerals in Contact with Cationic Surfactants." In Advances in Fine Particles Processing. Springer US, 1990. http://dx.doi.org/10.1007/978-1-4684-7959-1_14.

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Conference papers on the topic "Adsorption des cations"

1

Al Ezzi, Amged, and Hongbin Ma. "Equilibrium Adsorption Isotherm Mechanism of Water Vapor on Zeolites 3A, 4A, X, and Y." In ASME 2017 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2017. http://dx.doi.org/10.1115/imece2017-72601.

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Many researchers have analyzed the equilibrium adsorption isotherm mechanism of water vapor molecules on 4A, 3A, Y and X zeolites for decades. The demand for moisture removal continues to increase along with the increasing stringency of requirements for product quality control and production energy efficiency. Due to the negative charge of the zeolite framework, exchangeable compensation cations such as Na+, Li+, K+, Ba2+, Mg2+, and Ca2+ might be added. These cations are located at different sites within the framework and with different concentrations. Each cation shows a strong affinity to bo

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Chemerys, Valeriia, and Edita Baltrėnaitė. "Effect of Modification with FeCl3 and MgCl2 on Adsorption Characteristics of Woody Biochar." In Environmental Engineering. VGTU Technika, 2017. http://dx.doi.org/10.3846/enviro.2017.012.

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Due to high specific surface area, well-developed porous structure and surface functionality biochar has a potential for being used as low-cost adsorbent for adsorption of organic and inorganic contaminants from aqueous so-lutions. Higher adsorption capacity and selectivity for metals could be further developed after modification of proper-ties of biochar through physical (“designed biochar”) and chemical (“engineered biochar”) modification techniques. Wood waste of three types [aspen (Populus tremula L.), pine (Pinus sylvestris L.) and fir (Picea abies L.)] were se-lected to produce the bioch

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Wang, Qing, Valentina Prigiobbe, Chun Huh, Steven Lawrence Bryant, Kristian Mogensen, and Martin Vad Bennetzen. "Removal of Divalent Cations from Brine Using Selective Adsorption onto Magnetic Nanoparticles." In International Petroleum Technology Conference. International Petroleum Technology Conference, 2014. http://dx.doi.org/10.2523/iptc-17901-ms.

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Wang, Qing, Valentina Prigiobbe, Chun Huh, Steven Lawrence Bryant, Kristian Mogensen, and Martin Vad Bennetzen. "Removal of Divalent Cations from Brine Using Selective Adsorption onto Magnetic Nanoparticles." In International Petroleum Technology Conference. International Petroleum Technology Conference, 2014. http://dx.doi.org/10.2523/17901-ms.

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Yang, Peng, Jeffrey E. Post, Qian Wang, et al. "ADSORPTION OF METAL CATIONS AND OXYANIONS CONTROLS STABILITY OF LAYERED MANGANESE OXIDES." In GSA Annual Meeting in Phoenix, Arizona, USA - 2019. Geological Society of America, 2019. http://dx.doi.org/10.1130/abs/2019am-340237.

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Serincan, Mustafa Fazil, Ugur Pasaogullari, and Trent Molter. "Effect of Cathode Side Cationic Contamination on the Performance of an Operating PEFC." In ASME 2009 7th International Conference on Fuel Cell Science, Engineering and Technology. ASMEDC, 2009. http://dx.doi.org/10.1115/fuelcell2009-85229.

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A computational fluid dynamics model is developed to study the effect of cationic contamination on the performance of a polymer electrolyte fuel cell (PEFC). The fuel cell model incorporates mass, species, momentum and heat balances along with the ionic and electronic charge conservations. To model the transport of the cationic species, Nernst-Planck equations are used while taking into consideration of local electroneutrality in the ionomer phase. The diffusive fluxes of the cations are implemented in the Nernst-Planck equations such that they take into account adsorption of the species. A st

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Seok, Sangjun, and Doseok Kim. "Charge Inversion at the Surface by Adsorption of Trivalent Cations on Langmuir Monolayer." In 2007 Conference on Lasers and Electro-Optics - Pacific Rim. IEEE, 2007. http://dx.doi.org/10.1109/cleopr.2007.4391639.

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Pandova, Iveta. "TREATMENT OF WATER WITH RESPECT TO FERRIC CATIONS BY ADSORPTION ON A NATURAL ZEOLITE." In 19th SGEM International Multidisciplinary Scientific GeoConference EXPO Proceedings. STEF92 Technology, 2019. http://dx.doi.org/10.5593/sgem2019/3.1/s12.077.

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Pawlaczyk, Mateusz, and Grzegorz Schroeder. "Investigation of the Metal Cations Adsorption Selectivity Using Nanocavities-Rich Polyamine-Cross-Linked PMVEAMA." In The 6th World Congress on Recent Advances in Nanotechnology. Avestia Publishing, 2021. http://dx.doi.org/10.11159/icnnfc21.lx.103.

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Yamaguchi, Akiko, Masahiko Okumura, and Yoshio Takahashi. "Effect of Ionic Radius on the Adsorption Structure of Various Cations on 2:1 Clay Minerals." In Goldschmidt2020. Geochemical Society, 2020. http://dx.doi.org/10.46427/gold2020.2961.

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