Clay minerals are specified by permanent negative surface charge. In solutions of sodium salts, the surface of clay is covered by exchangeable sodium ions. In an acidic field (pH<4-6), sodium ions are displaced from the surface. This apparent H/Na exchange is conditioned by dissolution of alumina, followed by Al/Na exchange. Two kinds of published experimental data were considered in order to follow Al/Na exchange: the first is direct measurement of exchangeable sodium and aluminum in clay, and the second is exchange sorption of trace metal. Because of the equivalency of ionic exchange, trace metal acts as a probe, indicating the sodium content in clay. These experimental data were successfully modeled with use of the Poisson-Boltzmann equation, with the assumption that all exchange cations are located in the diffuse layer.
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http://dx.doi.org/10.1016/j.jcis.2009.04.018 | DOI Listing |
Chemosphere
January 2025
Departamento de Química, Universidade Federal do Paraná, 81531-980, Curitiba-PR, Brasil.
Soil is regarded as a natural repository for strongly adsorbed pollutants since glyphosate (GLY) is preferentially adsorbed by the inorganic fraction of the soil, which may greatly limits its leaching. In this way, understanding how clay mineralogy influences the sorption and transport processes of glyphosate in soils with different mineralogical characteristics is highly relevant. In this work, two clay mineralogy contrasting soils were used to evaluate GLY retention: a Oxisol (OX) with high levels of iron oxides (amorphous and crystalline) and a Inceptisol (IN) with a predominance of kaolinite.
View Article and Find Full Text PDFWater Res
December 2024
Department of Civil and Environmental Engineering, University of California, Berkeley, CA, 94720, United States. Electronic address:
Military bases and airports are often contaminated by per- and polyfluoroalkyl substances (PFAS) due to the repeated use of aqueous film forming foams (AFFFs) from decades of training exercises, equipment testing, and extinguishing of fuel- and solvent-based fires. Pump-and-treat systems combined with sorption processes are common ex situ remediation strategies; however, they can be expensive and may require decades of operation, particularly at sites where long-term diffusion and desorption of contaminants are the primary release processes. Alternatively, in situ chemical oxidation is an effective remediation strategy in which oxidants (e.
View Article and Find Full Text PDFChemosphere
December 2024
Department of Plant Biology and Ecology, Faculty of Biology, University of Bialystok, Ciolkowskiego 1J Street, 15-245, Bialystok, Poland.
Microplastics (MPs) in aquatic environments constitute an ideal surface for biofilm formation, facilitating or hindering the transport of contaminants. This study aims to provide knowledge on the sorption behavior of high-density polyethylene (μ-HDPE) after algal degradation toward UV filters. Up to now, the oxidation of μ-HDPE using the microalga Acutodesmus obliquus has not been studied.
View Article and Find Full Text PDFPolymers (Basel)
November 2024
Institute for Mechanics of Materials, University of Latvia, Jelgavas St. 3, LV-1004 Riga, Latvia.
This study investigated the moisture absorption and mechanical degradation of epoxy-based polymer systems with Mg-Al/NO layered double hydroxide (LDH) nanoparticles content up to 5 wt%. Such systems are developed for multilayer corrosion protective coatings. A sorption model was developed to calculate the moisture concentration field in the multilayer structures using Fick's law of diffusion.
View Article and Find Full Text PDFACS Omega
December 2024
Department of Chemical Engineering, Instituto de Ciências Ambientais, Químicas Farmacêuticas, Universidade Federal de São Paulo, Rua São Nicolau, 210, Diadema, Sao Paulo 09913-030, Brazil.
To enable the photoelectrocatalytic treatment of large volumes of water containing low concentrations of pollutants, this study introduces a hybrid photocatalyst, composed of nanotubular oxides grown on TiW alloy ( = 0.5 and 5.0 wt %) modified with UiO-66 MOF, for degradation of estrone (E1) and 17α-ethinyl estradiol (EE2).
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