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Nanospectroscopy Captures Nanoscale Compositional Zonation in Barite Solid Solutions

Scientists have long suspected that compositionally zoned particles can form under far-from equilibrium precipitation conditions, but their inferences have been based on bulk solid and solution measurements. We are the first to directly observe nanoscale trace element compositional zonation in <1...

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Autores principales: Ling, Florence T., Hunter, Heather A., Fitts, Jeffrey P., Peters, Catherine A., Acerbo, Alvin S., Huang, Xiaojing, Yan, Hanfei, Nazaretski, Evgeny, Chu, Yong S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6115454/
https://www.ncbi.nlm.nih.gov/pubmed/30158629
http://dx.doi.org/10.1038/s41598-018-31335-3
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author Ling, Florence T.
Hunter, Heather A.
Fitts, Jeffrey P.
Peters, Catherine A.
Acerbo, Alvin S.
Huang, Xiaojing
Yan, Hanfei
Nazaretski, Evgeny
Chu, Yong S.
author_facet Ling, Florence T.
Hunter, Heather A.
Fitts, Jeffrey P.
Peters, Catherine A.
Acerbo, Alvin S.
Huang, Xiaojing
Yan, Hanfei
Nazaretski, Evgeny
Chu, Yong S.
author_sort Ling, Florence T.
collection PubMed
description Scientists have long suspected that compositionally zoned particles can form under far-from equilibrium precipitation conditions, but their inferences have been based on bulk solid and solution measurements. We are the first to directly observe nanoscale trace element compositional zonation in <10 µm-sized particles using X-ray fluorescence nanospectroscopy at the Hard X-ray Nanoprobe (HXN) Beamline at National Synchrotron Light Source II (NSLS-II). Through high-resolution images, compositional zonation was observed in barite (BaSO(4)) particles precipitated from aqueous solution, in which Sr(2+) cations as well as HAsO(4)(2−) anions were co-precipitated into (Ba,Sr)SO(4) or Ba(SO(4),HAsO(4)) solid solutions. Under high salinity conditions (NaCl ≥ 1.0 M), bands contained ~3.5 to ~5 times more trace element compared to the center of the particle formed in early stages of particle growth. Quantitative analysis of Sr and As fractional substitution allowed us to determine that different crystallographic growth directions incorporated trace elements to different extents. These findings provide supporting evidence that barite solid solutions have great potential for trace element incorporation; this has significant implications for environmental and engineered systems that remove hazardous substances from water.
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spelling pubmed-61154542018-09-04 Nanospectroscopy Captures Nanoscale Compositional Zonation in Barite Solid Solutions Ling, Florence T. Hunter, Heather A. Fitts, Jeffrey P. Peters, Catherine A. Acerbo, Alvin S. Huang, Xiaojing Yan, Hanfei Nazaretski, Evgeny Chu, Yong S. Sci Rep Article Scientists have long suspected that compositionally zoned particles can form under far-from equilibrium precipitation conditions, but their inferences have been based on bulk solid and solution measurements. We are the first to directly observe nanoscale trace element compositional zonation in <10 µm-sized particles using X-ray fluorescence nanospectroscopy at the Hard X-ray Nanoprobe (HXN) Beamline at National Synchrotron Light Source II (NSLS-II). Through high-resolution images, compositional zonation was observed in barite (BaSO(4)) particles precipitated from aqueous solution, in which Sr(2+) cations as well as HAsO(4)(2−) anions were co-precipitated into (Ba,Sr)SO(4) or Ba(SO(4),HAsO(4)) solid solutions. Under high salinity conditions (NaCl ≥ 1.0 M), bands contained ~3.5 to ~5 times more trace element compared to the center of the particle formed in early stages of particle growth. Quantitative analysis of Sr and As fractional substitution allowed us to determine that different crystallographic growth directions incorporated trace elements to different extents. These findings provide supporting evidence that barite solid solutions have great potential for trace element incorporation; this has significant implications for environmental and engineered systems that remove hazardous substances from water. Nature Publishing Group UK 2018-08-29 /pmc/articles/PMC6115454/ /pubmed/30158629 http://dx.doi.org/10.1038/s41598-018-31335-3 Text en © The Author(s) 2018 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
Ling, Florence T.
Hunter, Heather A.
Fitts, Jeffrey P.
Peters, Catherine A.
Acerbo, Alvin S.
Huang, Xiaojing
Yan, Hanfei
Nazaretski, Evgeny
Chu, Yong S.
Nanospectroscopy Captures Nanoscale Compositional Zonation in Barite Solid Solutions
title Nanospectroscopy Captures Nanoscale Compositional Zonation in Barite Solid Solutions
title_full Nanospectroscopy Captures Nanoscale Compositional Zonation in Barite Solid Solutions
title_fullStr Nanospectroscopy Captures Nanoscale Compositional Zonation in Barite Solid Solutions
title_full_unstemmed Nanospectroscopy Captures Nanoscale Compositional Zonation in Barite Solid Solutions
title_short Nanospectroscopy Captures Nanoscale Compositional Zonation in Barite Solid Solutions
title_sort nanospectroscopy captures nanoscale compositional zonation in barite solid solutions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6115454/
https://www.ncbi.nlm.nih.gov/pubmed/30158629
http://dx.doi.org/10.1038/s41598-018-31335-3
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