The Influence of Aqueous Se(IV) on the Stability of Different CaCO<sub>3</sub> Polymorphs Precipitated under Ambient Conditions

Selenium is an essential bio-element, but because of its bioaccumulation potential, it can become toxic and is an important pollutant. The ubiquitous mineral calcite (CaCO<sub>3</sub>) has the ability to immobilize anions as SeO<sub>3</sub><sup>2−</sup> by differe...

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Autores principales: Angeles Fernandez-Gonzalez, Alba Lozano-Letellier, Begoña Fernandez
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Publicado: MDPI AG 2021
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spelling oai:doaj.org-article:8b93eeda16af44ce8c94d0a159e904082021-11-25T18:26:30ZThe Influence of Aqueous Se(IV) on the Stability of Different CaCO<sub>3</sub> Polymorphs Precipitated under Ambient Conditions10.3390/min111112382075-163Xhttps://doaj.org/article/8b93eeda16af44ce8c94d0a159e904082021-11-01T00:00:00Zhttps://www.mdpi.com/2075-163X/11/11/1238https://doaj.org/toc/2075-163XSelenium is an essential bio-element, but because of its bioaccumulation potential, it can become toxic and is an important pollutant. The ubiquitous mineral calcite (CaCO<sub>3</sub>) has the ability to immobilize anions as SeO<sub>3</sub><sup>2−</sup> by different sorption or coprecipitation processes. Experimental studies have found that SeO<sub>3</sub><sup>2−</sup> can incorporate in the crystal structure of calcite by substituting CO<sub>3</sub><sup>2−</sup>. The presence of foreign ions in aqueous solution strongly affects CaCO<sub>3</sub> precipitation, helping stabilize less stable polymorphs such as vaterite and aragonite or hydrated phases. In this work, we studied the aging process of calcium carbonates precipitated from aqueous solutions highly supersaturated with respect to CaCO<sub>3</sub> and slightly supersaturated with respect to CaSeO<sub>3</sub>·H<sub>2</sub>O under ambient conditions, for times up to 30 days in which solids were kept in the remaining aqueous solution. Under these conditions, CaCO<sub>3</sub> precipitated mainly as low crystallinity vaterite aggregates that hosted up to 16% atomic ratio Se:C. Vaterite purified and increased its crystallinity with aging time, but the vaterite–calcite transformation was strongly inhibited. The incorporation of Se(IV) in vaterite did not significantly affect the cell parameters or the external morphology of the aggregates. The precipitation of selenite as CaSeO<sub>3</sub>·H<sub>2</sub>O was conditioned by the availability of free Ca<sup>2+</sup> and SeO<sub>3</sub><sup>2−</sup> that was not previously incorporated into precipitated carbonates.Angeles Fernandez-GonzalezAlba Lozano-LetellierBegoña FernandezMDPI AGarticlecalcium carbonate polymorphismselenitecalcium carbonate precipitationvateriteMineralogyQE351-399.2ENMinerals, Vol 11, Iss 1238, p 1238 (2021)
institution DOAJ
collection DOAJ
language EN
topic calcium carbonate polymorphism
selenite
calcium carbonate precipitation
vaterite
Mineralogy
QE351-399.2
spellingShingle calcium carbonate polymorphism
selenite
calcium carbonate precipitation
vaterite
Mineralogy
QE351-399.2
Angeles Fernandez-Gonzalez
Alba Lozano-Letellier
Begoña Fernandez
The Influence of Aqueous Se(IV) on the Stability of Different CaCO<sub>3</sub> Polymorphs Precipitated under Ambient Conditions
description Selenium is an essential bio-element, but because of its bioaccumulation potential, it can become toxic and is an important pollutant. The ubiquitous mineral calcite (CaCO<sub>3</sub>) has the ability to immobilize anions as SeO<sub>3</sub><sup>2−</sup> by different sorption or coprecipitation processes. Experimental studies have found that SeO<sub>3</sub><sup>2−</sup> can incorporate in the crystal structure of calcite by substituting CO<sub>3</sub><sup>2−</sup>. The presence of foreign ions in aqueous solution strongly affects CaCO<sub>3</sub> precipitation, helping stabilize less stable polymorphs such as vaterite and aragonite or hydrated phases. In this work, we studied the aging process of calcium carbonates precipitated from aqueous solutions highly supersaturated with respect to CaCO<sub>3</sub> and slightly supersaturated with respect to CaSeO<sub>3</sub>·H<sub>2</sub>O under ambient conditions, for times up to 30 days in which solids were kept in the remaining aqueous solution. Under these conditions, CaCO<sub>3</sub> precipitated mainly as low crystallinity vaterite aggregates that hosted up to 16% atomic ratio Se:C. Vaterite purified and increased its crystallinity with aging time, but the vaterite–calcite transformation was strongly inhibited. The incorporation of Se(IV) in vaterite did not significantly affect the cell parameters or the external morphology of the aggregates. The precipitation of selenite as CaSeO<sub>3</sub>·H<sub>2</sub>O was conditioned by the availability of free Ca<sup>2+</sup> and SeO<sub>3</sub><sup>2−</sup> that was not previously incorporated into precipitated carbonates.
format article
author Angeles Fernandez-Gonzalez
Alba Lozano-Letellier
Begoña Fernandez
author_facet Angeles Fernandez-Gonzalez
Alba Lozano-Letellier
Begoña Fernandez
author_sort Angeles Fernandez-Gonzalez
title The Influence of Aqueous Se(IV) on the Stability of Different CaCO<sub>3</sub> Polymorphs Precipitated under Ambient Conditions
title_short The Influence of Aqueous Se(IV) on the Stability of Different CaCO<sub>3</sub> Polymorphs Precipitated under Ambient Conditions
title_full The Influence of Aqueous Se(IV) on the Stability of Different CaCO<sub>3</sub> Polymorphs Precipitated under Ambient Conditions
title_fullStr The Influence of Aqueous Se(IV) on the Stability of Different CaCO<sub>3</sub> Polymorphs Precipitated under Ambient Conditions
title_full_unstemmed The Influence of Aqueous Se(IV) on the Stability of Different CaCO<sub>3</sub> Polymorphs Precipitated under Ambient Conditions
title_sort influence of aqueous se(iv) on the stability of different caco<sub>3</sub> polymorphs precipitated under ambient conditions
publisher MDPI AG
publishDate 2021
url https://doaj.org/article/8b93eeda16af44ce8c94d0a159e90408
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