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Adsorption of phosphate on iron oxide doped halloysite nanotubes

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 nanoclay...

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Autores principales: Almasri, Dema A., Saleh, Navid B., Atieh, Muataz A., McKay, Gordon, Ahzi, Said
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6397243/
https://www.ncbi.nlm.nih.gov/pubmed/30824719
http://dx.doi.org/10.1038/s41598-019-39035-2
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author Almasri, Dema A.
Saleh, Navid B.
Atieh, Muataz A.
McKay, Gordon
Ahzi, Said
author_facet Almasri, Dema A.
Saleh, Navid B.
Atieh, Muataz A.
McKay, Gordon
Ahzi, Said
author_sort Almasri, Dema A.
collection PubMed
description 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(2)O(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(2)O(3)) modified HNTs (Fe-HNT) is conducted. Influences of Fe(2)O(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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spelling pubmed-63972432019-03-05 Adsorption of phosphate on iron oxide doped halloysite nanotubes Almasri, Dema A. Saleh, Navid B. Atieh, Muataz A. McKay, Gordon Ahzi, Said Sci Rep Article 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(2)O(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(2)O(3)) modified HNTs (Fe-HNT) is conducted. Influences of Fe(2)O(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. Nature Publishing Group UK 2019-03-01 /pmc/articles/PMC6397243/ /pubmed/30824719 http://dx.doi.org/10.1038/s41598-019-39035-2 Text en © 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/.
spellingShingle Article
Almasri, Dema A.
Saleh, Navid B.
Atieh, Muataz A.
McKay, Gordon
Ahzi, Said
Adsorption of phosphate on iron oxide doped halloysite nanotubes
title Adsorption of phosphate on iron oxide doped halloysite nanotubes
title_full Adsorption of phosphate on iron oxide doped halloysite nanotubes
title_fullStr Adsorption of phosphate on iron oxide doped halloysite nanotubes
title_full_unstemmed Adsorption of phosphate on iron oxide doped halloysite nanotubes
title_short Adsorption of phosphate on iron oxide doped halloysite nanotubes
title_sort adsorption of phosphate on iron oxide doped halloysite nanotubes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6397243/
https://www.ncbi.nlm.nih.gov/pubmed/30824719
http://dx.doi.org/10.1038/s41598-019-39035-2
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