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Chrysotile asbestos treated with phosphoric acid as an adsorbent for ammonia nitrogen

The purpose of this study was to find an alternative application for chrysotile asbestos, given that there is a complete structure of extraction and production of this class of serpentine minerals, but its use is banned for many applications. The idea was to obtain a compound that could immobilize p...

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Autores principales: Girotto, Camila P., de Campos, Sílvia D., de Campos, Élvio A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7030997/
https://www.ncbi.nlm.nih.gov/pubmed/32099924
http://dx.doi.org/10.1016/j.heliyon.2020.e03397
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author Girotto, Camila P.
de Campos, Sílvia D.
de Campos, Élvio A.
author_facet Girotto, Camila P.
de Campos, Sílvia D.
de Campos, Élvio A.
author_sort Girotto, Camila P.
collection PubMed
description The purpose of this study was to find an alternative application for chrysotile asbestos, given that there is a complete structure of extraction and production of this class of serpentine minerals, but its use is banned for many applications. The idea was to obtain a compound that could immobilize phosphate by triggering a reaction between the magnesium oxide and hydroxide contained in the mineral, without causing phosphate leaching. To this end, chrysotile (Mg(3)SiO(5)(OH)(4)) was treated with phosphoric acid (H(3)PO(4)) in a molar ratio of 1:3 in an aqueous medium at 85 °C until the solvent evaporated, resulting in two different solid compounds, which were prepared in a similar manner. The first compound (cri/H(3)PO(4) 1:3)(1), was obtained by rinsing and then heat-treating it at 150 °C for 6 h, while the second one, (cri/H(3)PO(4) 1:3)(2), was rinsed after the heat treatment. Compound (cri/H(3)PO(4) 1:3)(1) underwent partial leaching, while compound (cri/H(3)PO(4) 1:3)(2) showed a mass increase of 48%, with the formation of crystalline magnesium pyrophosphate mixed with amorphous SiO(2). The latter compound adsorbed N–NH(3) at pH 10, following the pseudo-first-order model (activation energy = 8329 ± 1696 J mol(−1)). Equilibrium experiments, which were performed following Hill's sigmoidal type S2 isotherm model, indicated that the adsorption phenomenon was governed by two processes, i.e., complexation up to the inflection point (K(H) between 10.0 mg L(−1) at 40 °C and 13.6 mg L(−1) at 25 °C) followed by adsorption. The q(max) varied from 18.0 to 19.6 mgN g(−1) and the adsorbent was reusable, maintaining its initial adsorbent capacity during its first reuse. This material, which was tested on real effluents, presented a N–NH(3) removal rate similar to that shown by the test solutions. The treatment of chrysotile with H(3)PO(4) conducts it to a composite that adsorbs ammoniacal nitrogen at pH 10 and it is reusable maintaining the adsorption capacity.
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spelling pubmed-70309972020-02-25 Chrysotile asbestos treated with phosphoric acid as an adsorbent for ammonia nitrogen Girotto, Camila P. de Campos, Sílvia D. de Campos, Élvio A. Heliyon Article The purpose of this study was to find an alternative application for chrysotile asbestos, given that there is a complete structure of extraction and production of this class of serpentine minerals, but its use is banned for many applications. The idea was to obtain a compound that could immobilize phosphate by triggering a reaction between the magnesium oxide and hydroxide contained in the mineral, without causing phosphate leaching. To this end, chrysotile (Mg(3)SiO(5)(OH)(4)) was treated with phosphoric acid (H(3)PO(4)) in a molar ratio of 1:3 in an aqueous medium at 85 °C until the solvent evaporated, resulting in two different solid compounds, which were prepared in a similar manner. The first compound (cri/H(3)PO(4) 1:3)(1), was obtained by rinsing and then heat-treating it at 150 °C for 6 h, while the second one, (cri/H(3)PO(4) 1:3)(2), was rinsed after the heat treatment. Compound (cri/H(3)PO(4) 1:3)(1) underwent partial leaching, while compound (cri/H(3)PO(4) 1:3)(2) showed a mass increase of 48%, with the formation of crystalline magnesium pyrophosphate mixed with amorphous SiO(2). The latter compound adsorbed N–NH(3) at pH 10, following the pseudo-first-order model (activation energy = 8329 ± 1696 J mol(−1)). Equilibrium experiments, which were performed following Hill's sigmoidal type S2 isotherm model, indicated that the adsorption phenomenon was governed by two processes, i.e., complexation up to the inflection point (K(H) between 10.0 mg L(−1) at 40 °C and 13.6 mg L(−1) at 25 °C) followed by adsorption. The q(max) varied from 18.0 to 19.6 mgN g(−1) and the adsorbent was reusable, maintaining its initial adsorbent capacity during its first reuse. This material, which was tested on real effluents, presented a N–NH(3) removal rate similar to that shown by the test solutions. The treatment of chrysotile with H(3)PO(4) conducts it to a composite that adsorbs ammoniacal nitrogen at pH 10 and it is reusable maintaining the adsorption capacity. Elsevier 2020-02-18 /pmc/articles/PMC7030997/ /pubmed/32099924 http://dx.doi.org/10.1016/j.heliyon.2020.e03397 Text en © 2020 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
Girotto, Camila P.
de Campos, Sílvia D.
de Campos, Élvio A.
Chrysotile asbestos treated with phosphoric acid as an adsorbent for ammonia nitrogen
title Chrysotile asbestos treated with phosphoric acid as an adsorbent for ammonia nitrogen
title_full Chrysotile asbestos treated with phosphoric acid as an adsorbent for ammonia nitrogen
title_fullStr Chrysotile asbestos treated with phosphoric acid as an adsorbent for ammonia nitrogen
title_full_unstemmed Chrysotile asbestos treated with phosphoric acid as an adsorbent for ammonia nitrogen
title_short Chrysotile asbestos treated with phosphoric acid as an adsorbent for ammonia nitrogen
title_sort chrysotile asbestos treated with phosphoric acid as an adsorbent for ammonia nitrogen
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7030997/
https://www.ncbi.nlm.nih.gov/pubmed/32099924
http://dx.doi.org/10.1016/j.heliyon.2020.e03397
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