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Fe(III)-polyhydroxy cations supported onto K10 montmorillonite for removal of phosphate from waters

Since phosphate is strongly related to eutrophication of environmental waters, several research groups quest for materials that can efficiently remove phosphate from wastewaters before it contaminates lakes and reservoirs. In the present work, a commercial clay mineral (K10 montmorillonite) modified...

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Autores principales: Leite, Samara T., do Nascimento, Fernando H., Masini, Jorge C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7195538/
https://www.ncbi.nlm.nih.gov/pubmed/32373749
http://dx.doi.org/10.1016/j.heliyon.2020.e03868
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author Leite, Samara T.
do Nascimento, Fernando H.
Masini, Jorge C.
author_facet Leite, Samara T.
do Nascimento, Fernando H.
Masini, Jorge C.
author_sort Leite, Samara T.
collection PubMed
description Since phosphate is strongly related to eutrophication of environmental waters, several research groups quest for materials that can efficiently remove phosphate from wastewaters before it contaminates lakes and reservoirs. In the present work, a commercial clay mineral (K10 montmorillonite) modified with Fe(3+) polyhydroxy cations was investigated as an adsorbent for phosphate. The incorporation of the polycations did not alter the main conformational characteristics of the montmorillonite, as verified by specific surface area measurements, X-ray diffractometry, FTIR, electron microscopy, and zeta potential titrations. On the other hand, the materials supporting Fe(3+) polyhydroxy cations exhibited a significant enhancement of adsorption capacity, as determined by Langmuir-Freundlich isotherms, from 39 ± 2 to 104 ± 15 μmol g(−1). The different ratios of OH(−) to Fe(3+) did not affect the adsorption capacities. The adsorption kinetics was best described by the pseudo 2(nd) order model, approaching the equilibrium after 120 min of contact time. A variation of pH between 4.6 and 8.5 did not affect the adsorption percentages. The adsorption capacities increased with the increase of the ionic strength, thus suggesting that the formation of inner-sphere complexes prevails over electrostatic interactions as the adsorption mechanism. The materials removed phosphate from three polluted water samples having phosphate concentrations between 0.0919 and 1.211 mg L(−1). The remaining phosphate concentration was below the limit of quantification of the analytical method (0.063 mg L(−1) in P, or 2.0 μmol L(−1)). The presence of 10 mg L(−1) humic of fulvic acid did not affect the performance of the materials. In conclusion, the modification of clay minerals with Fe(3+) polyhydroxy cations is useful in producing low-cost adsorbents for phosphate.
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spelling pubmed-71955382020-05-05 Fe(III)-polyhydroxy cations supported onto K10 montmorillonite for removal of phosphate from waters Leite, Samara T. do Nascimento, Fernando H. Masini, Jorge C. Heliyon Article Since phosphate is strongly related to eutrophication of environmental waters, several research groups quest for materials that can efficiently remove phosphate from wastewaters before it contaminates lakes and reservoirs. In the present work, a commercial clay mineral (K10 montmorillonite) modified with Fe(3+) polyhydroxy cations was investigated as an adsorbent for phosphate. The incorporation of the polycations did not alter the main conformational characteristics of the montmorillonite, as verified by specific surface area measurements, X-ray diffractometry, FTIR, electron microscopy, and zeta potential titrations. On the other hand, the materials supporting Fe(3+) polyhydroxy cations exhibited a significant enhancement of adsorption capacity, as determined by Langmuir-Freundlich isotherms, from 39 ± 2 to 104 ± 15 μmol g(−1). The different ratios of OH(−) to Fe(3+) did not affect the adsorption capacities. The adsorption kinetics was best described by the pseudo 2(nd) order model, approaching the equilibrium after 120 min of contact time. A variation of pH between 4.6 and 8.5 did not affect the adsorption percentages. The adsorption capacities increased with the increase of the ionic strength, thus suggesting that the formation of inner-sphere complexes prevails over electrostatic interactions as the adsorption mechanism. The materials removed phosphate from three polluted water samples having phosphate concentrations between 0.0919 and 1.211 mg L(−1). The remaining phosphate concentration was below the limit of quantification of the analytical method (0.063 mg L(−1) in P, or 2.0 μmol L(−1)). The presence of 10 mg L(−1) humic of fulvic acid did not affect the performance of the materials. In conclusion, the modification of clay minerals with Fe(3+) polyhydroxy cations is useful in producing low-cost adsorbents for phosphate. Elsevier 2020-04-28 /pmc/articles/PMC7195538/ /pubmed/32373749 http://dx.doi.org/10.1016/j.heliyon.2020.e03868 Text en © 2020 The Authors. Published by Elsevier Ltd. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Leite, Samara T.
do Nascimento, Fernando H.
Masini, Jorge C.
Fe(III)-polyhydroxy cations supported onto K10 montmorillonite for removal of phosphate from waters
title Fe(III)-polyhydroxy cations supported onto K10 montmorillonite for removal of phosphate from waters
title_full Fe(III)-polyhydroxy cations supported onto K10 montmorillonite for removal of phosphate from waters
title_fullStr Fe(III)-polyhydroxy cations supported onto K10 montmorillonite for removal of phosphate from waters
title_full_unstemmed Fe(III)-polyhydroxy cations supported onto K10 montmorillonite for removal of phosphate from waters
title_short Fe(III)-polyhydroxy cations supported onto K10 montmorillonite for removal of phosphate from waters
title_sort fe(iii)-polyhydroxy cations supported onto k10 montmorillonite for removal of phosphate from waters
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7195538/
https://www.ncbi.nlm.nih.gov/pubmed/32373749
http://dx.doi.org/10.1016/j.heliyon.2020.e03868
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