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      Adsorption of phosphate on iron oxide doped halloysite nanotubes

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          Abstract

          Excess phosphate in water is known to cause eutrophication, and its removal is imperative. Nanoclay minerals are widely used in environmental remediation due to their low-cost, adequate availability, environmental compatibility, and adsorption efficiency. However, the removal of anions with nanoclays is not very effective because of electrostatic repulsion from clay surfaces with a net negative charge. Among clay minerals, halloysite nanotubes (HNTs) possess a negatively charged exterior and a positively charged inner lumen. This provides an increased affinity for anion removal. In this study, HNTs are modified with nano-scale iron oxide (Fe 2O 3) to enhance the adsorption capacity of the nanosorbent. This modification allowed for effective distribution of these oxide surfaces, which are known to sorb phosphate via ligand exchange and by forming inner-sphere complexes. A detailed characterization of the raw and (Fe 2O 3) modified HNTs (Fe-HNT) is conducted. Influences of Fe 2O 3 loading, adsorbent dosage, contact time, pH, initial phosphate concentration, and coexisting ions on the phosphate adsorption capacity are studied. Results demonstrate that adsorption on Fe-HNT is pH-dependent with fast initial adsorption kinetics. The underlying mechanism is identified as a combination of electrostatic attraction, ligand exchange, and Lewis acid-base interactions. The nanomaterial provides promising results for its application in water/wastewater treatment.

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          Kinetics of Adsorption on Carbon from Solution

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            Review of second-order models for adsorption systems.

            Applications of second-order kinetic models to adsorption systems were reviewed. An overview of second-order kinetic expressions is described in this paper based on the solid adsorption capacity. An early empirical second-order equation was applied in the adsorption of gases onto a solid. A similar second-order equation was applied to describe ion exchange reactions. In recent years, a pseudo-second-order rate expression has been widely applied to the adsorption of pollutants from aqueous solutions onto adsorbents. In addition, the earliest rate equation based on the solid adsorption capacity is also presented in detail.
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              A Comparison of Chemisorption Kinetic Models Applied to Pollutant Removal on Various Sorbents

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                Author and article information

                Contributors
                mhussein@hbku.edu.qa
                sahzi@hbku.edu.qa
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                1 March 2019
                1 March 2019
                2019
                : 9
                : 3232
                Affiliations
                [1 ]ISNI 0000 0001 0516 2170, GRID grid.418818.c, Qatar Environment and Energy Research Institute (QEERI), , Hamad Bin Khalifa University (HBKU), Qatar Foundation, ; PO Box 34110, Doha, Qatar
                [2 ]ISNI 0000 0001 0516 2170, GRID grid.418818.c, College of Science and Engineering, , Hamad Bin Khalifa University, Qatar Foundation, ; PO Box 34110, Doha, Qatar
                [3 ]ISNI 0000000121548364, GRID grid.55460.32, Department of Civil, Architectural and Environmental Engineering, , University of Texas, ; Austin, TX 78712 USA
                Article
                39035
                10.1038/s41598-019-39035-2
                6397243
                30824719
                50b1c1ac-56ec-4fc9-b3ef-dd51f925a616
                © The Author(s) 2019

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 9 September 2018
                : 15 November 2018
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