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Soil Systems
Special Issues
Adsorption Processes in Soils and Sediments
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Adsorption Processes in Soils and Sediments

A special issue of Soil Systems (ISSN 2571-8789).

Deadline for manuscript submissions: 30 June 2025 | Viewed by 1746

Special Issue Editor

Dr. Sudipta Rakshit

E-Mail Website
Guest Editor
Department of Agricultural and Environmental Sciences, Tennessee State University, Nashville, TN 37209, USA
Interests: fate of emerging contaminants: pharmaceuticals and metalloids (antimony); nutrient cycling (nitrogen and phosphorus); redox biogeochemistry of humic substances; environmental remediation

Special Issue Information

Dear Colleagues,

Adsorption processes in soil and sediments influence the partitioning of nutrient oxyanions, cations, and pollutant ions between solid (soil) and liquid (water) phases and thus change their mobility in the ecosystem. Understanding the adsorption mechanisms of nutrient and pollutant ions is a key to predicting their fate in the environment. Various other factors and processes can also affect the partitioning mechanisms. For example, oxidation/reduction processes, the presence of co-adsorbing or competing ions, microbial activity, temperature fluctuations, etc.

Authors are invited to submit their manuscripts on the adsorption mechanisms of nutrient or pollutant ions on soils, sediments, or environmentally relevant synthetic soil minerals. The research can be focused on only macroscopic adsorption study or with the detailed spectroscopic characterizations of the mechanisms or a combination of both.

Dr. Sudipta Rakshit
Guest Editor

Manuscript Submission Information

Manuscripts should be submitted online at www.mdpi.com by registering and logging in to this website. Once you are registered, click here to go to the submission form. Manuscripts can be submitted until the deadline. All submissions that pass pre-check are peer-reviewed. Accepted papers will be published continuously in the journal (as soon as accepted) and will be listed together on the special issue website. Research articles, review articles as well as short communications are invited. For planned papers, a title and short abstract (about 100 words) can be sent to the Editorial Office for announcement on this website.

Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are thoroughly refereed through a single-blind peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page. Soil Systems is an international peer-reviewed open access quarterly journal published by MDPI.

Please visit the Instructions for Authors page before submitting a manuscript. The Article Processing Charge (APC) for publication in this open access journal is 1800 CHF (Swiss Francs). Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.

Keywords

  • adsorption processes
  • soils
  • sediments

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Published Papers (2 papers)

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Research

23 pages, 2901 KiB  
Article
Wood Gasification Biochar as an Effective Biosorbent for the Remediation of Organic Soil Pollutants
by Elisabetta Loffredo, Nicola Denora, Danilo Vona, Antonio Gelsomino, Carlo Porfido and Nicola Colatorti
Soil Syst. 2025, 9(1), 18; https://doi.org/10.3390/soilsystems9010018 - 24 Feb 2025
Abstract
A biochar (BC) generated by the pyrogasification of wood chips from authorized forestry cuts was extensively characterized and evaluated for its efficacy in retaining/releasing two agrochemicals, namely the fungicide penconazole (PEN), the herbicide S-metolachlor (S-MET), and the xenoestrogen bisphenol A (BPA) widely present [...] Read more.
A biochar (BC) generated by the pyrogasification of wood chips from authorized forestry cuts was extensively characterized and evaluated for its efficacy in retaining/releasing two agrochemicals, namely the fungicide penconazole (PEN), the herbicide S-metolachlor (S-MET), and the xenoestrogen bisphenol A (BPA) widely present in industrial effluents. The elemental composition of BC was evaluated using CN elemental analysis and total reflection X-ray fluorescence (TXRF) spectroscopy which showed the abundance of elements typically found in BCs (Ca, K, P) along with essential trace elements such as Fe and Mn. Scanning electron microscopy coupled with energy-dispersive X-ray analysis (SEM-EDX) described the surface features of BC along with the major surface elements, while Brunauer–Emmett–Teller (BET) analysis revealed, as expected, a large specific surface area (366 m2 g−1). High porosity (0.07 cm3 g−1) was demonstrated by the density functional theory (DFT) method, while Fourier transform infrared (FT-IR) spectroscopy highlighted the presence of a prominent aromatic structure and the abundance of reactive functional groups responsible for the binding of the compounds. The sorption/desorption capacity of BC was studied by means of sorption kinetics and isotherms in batch trials, and by modeling the experimental data with various theoretical equations. All compounds reached sorption equilibrium on BC very rapidly, following preferentially pseudo-second-order kinetics. Freundlich adsorption constants of PEN, S-MET, and BPA were 37.3, 13.2, and 11.6 L g−1, respectively, thus demonstrating the great affinity of BC for hydrophobic pollutants. The adsorption process was hysteretic as only a small fraction of each compound was slowly desorbed from BC. The overall results obtained highlighted the great potential of BC of acting as a biosorbent of contaminants, which is of great importance for the containment of pollution in agricultural soils and for limiting the entry of toxic compounds into the human and animal food chain. Full article
(This article belongs to the Special Issue Adsorption Processes in Soils and Sediments)
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17 pages, 4336 KiB  
Article
Sorption and Phase Associations of Chromate and Vanadate with Two Contrasting North Carolina Saprolites
by Fatai O. Balogun, Hannah R. Peel, Robert E. Austin, Ibrahim G. Okunlola, David S. Vinson, Owen W. Duckworth and Matthew L. Polizzotto
Soil Syst. 2024, 8(4), 127; https://doi.org/10.3390/soilsystems8040127 - 3 Dec 2024
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Abstract
Geogenic chromium (Cr) and vanadium (V) contamination of groundwater in the Piedmont region of North Carolina poses threats to public health. These contaminants are naturally derived from saprolite and aquifer materials, but geochemical variability in these materials makes it difficult to predict specific [...] Read more.
Geogenic chromium (Cr) and vanadium (V) contamination of groundwater in the Piedmont region of North Carolina poses threats to public health. These contaminants are naturally derived from saprolite and aquifer materials, but geochemical variability in these materials makes it difficult to predict specific risks of Cr and V in well water. The objectives of this study were to (1) determine host phases of Cr and V in representative subsurface materials; (2) characterize contaminant binding parameters of chemically variable saprolites; and (3) examine the influence of saprolite chemistry on contaminant sorption, speciation, and phase associations. Isotherm experiments revealed that saprolite samples sorbed roughly an order of magnitude more V than Cr. Chemical extractions and synchrotron-based X-ray fluorescence showed that substantial Cr and V were bound with metal oxide/oxyhydroxides in native and Cr-and V-sorbed saprolites; however, electrostatically bound fractions were also present, representing potentially important sources of groundwater contamination. X-ray absorption-near-edge-structure spectroscopy indicated that sorbed Cr was found as reduced Cr(III), whereas sorbed V was dominated by the oxidized V(V) and intermediate V(IV) species. Results from this study could be used to help parameterize mechanistic models and improve prediction of the Cr and V contamination potential of shallow aquifers. Full article
(This article belongs to the Special Issue Adsorption Processes in Soils and Sediments)
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