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Structure and phase analysis of calcium carbonate powder prepared by a simple solution method
This paper focused on the analysis of the crystal structure and phase transformation of CaCO(3) synthesized by simple solution method from 0.5 M Ca(NO(3))(2) precursor and 0.5 M Na(2)CO(3) precipitant at ambient temperature (300 K). The pH of the sample solution at various reaction times of 5, 10, 1...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8593454/ https://www.ncbi.nlm.nih.gov/pubmed/34816040 http://dx.doi.org/10.1016/j.heliyon.2021.e08344 |
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author | Febrida, Renny Setianto, Setianto Herda, Ellyza Cahyanto, Arief Joni, I Made |
author_facet | Febrida, Renny Setianto, Setianto Herda, Ellyza Cahyanto, Arief Joni, I Made |
author_sort | Febrida, Renny |
collection | PubMed |
description | This paper focused on the analysis of the crystal structure and phase transformation of CaCO(3) synthesized by simple solution method from 0.5 M Ca(NO(3))(2) precursor and 0.5 M Na(2)CO(3) precipitant at ambient temperature (300 K). The pH of the sample solution at various reaction times of 5, 10, 15, and 30 min were measured and correlated with the supersaturating condition in the presence of the Na(2)CO(3) which is responsible for vaterite phase formation. The formation of the polymorph structure of obtained CaCO(3) powders was characterized using powder X-ray diffraction patterns and their crystal structure and phase transformation were evaluated using the Rietveld refinement method. Moreover, the qualitative analysis of the CaCO(3) powders phase was conducted by Fourier Transform Infrared (FTIR) spectroscopy to evaluate the effect of reaction time correlated with their crystal formation. The XRD analysis showed that the vaterite formation was 89 % at a reaction time of 15 min and confirmed also by FTIR that the amount of vaterite increased due to the effect of increasing reaction time. The crystallite size of vaterite was stable at 36 nm at the reaction time of 15 and 30 min. The morphology of the CaCO(3) powders obtained from Scanning Electron Microscope (SEM) was spherical with sizes of 2–5 μm. It was highlighted that the supersaturating condition started occurred at a reaction time of 15 min at pH 7.88 which was responsible for vaterite formation took place. It was concluded that the amount of precipitant (Na(2)CO(3)) and reaction times play an important role to determine the saturation of carbonate source to allow vaterite phase formation of CaCO(3) powders to occur. |
format | Online Article Text |
id | pubmed-8593454 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-85934542021-11-22 Structure and phase analysis of calcium carbonate powder prepared by a simple solution method Febrida, Renny Setianto, Setianto Herda, Ellyza Cahyanto, Arief Joni, I Made Heliyon Research Article This paper focused on the analysis of the crystal structure and phase transformation of CaCO(3) synthesized by simple solution method from 0.5 M Ca(NO(3))(2) precursor and 0.5 M Na(2)CO(3) precipitant at ambient temperature (300 K). The pH of the sample solution at various reaction times of 5, 10, 15, and 30 min were measured and correlated with the supersaturating condition in the presence of the Na(2)CO(3) which is responsible for vaterite phase formation. The formation of the polymorph structure of obtained CaCO(3) powders was characterized using powder X-ray diffraction patterns and their crystal structure and phase transformation were evaluated using the Rietveld refinement method. Moreover, the qualitative analysis of the CaCO(3) powders phase was conducted by Fourier Transform Infrared (FTIR) spectroscopy to evaluate the effect of reaction time correlated with their crystal formation. The XRD analysis showed that the vaterite formation was 89 % at a reaction time of 15 min and confirmed also by FTIR that the amount of vaterite increased due to the effect of increasing reaction time. The crystallite size of vaterite was stable at 36 nm at the reaction time of 15 and 30 min. The morphology of the CaCO(3) powders obtained from Scanning Electron Microscope (SEM) was spherical with sizes of 2–5 μm. It was highlighted that the supersaturating condition started occurred at a reaction time of 15 min at pH 7.88 which was responsible for vaterite formation took place. It was concluded that the amount of precipitant (Na(2)CO(3)) and reaction times play an important role to determine the saturation of carbonate source to allow vaterite phase formation of CaCO(3) powders to occur. Elsevier 2021-11-08 /pmc/articles/PMC8593454/ /pubmed/34816040 http://dx.doi.org/10.1016/j.heliyon.2021.e08344 Text en © 2021 The Author(s) https://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 | Research Article Febrida, Renny Setianto, Setianto Herda, Ellyza Cahyanto, Arief Joni, I Made Structure and phase analysis of calcium carbonate powder prepared by a simple solution method |
title | Structure and phase analysis of calcium carbonate powder prepared by a simple solution method |
title_full | Structure and phase analysis of calcium carbonate powder prepared by a simple solution method |
title_fullStr | Structure and phase analysis of calcium carbonate powder prepared by a simple solution method |
title_full_unstemmed | Structure and phase analysis of calcium carbonate powder prepared by a simple solution method |
title_short | Structure and phase analysis of calcium carbonate powder prepared by a simple solution method |
title_sort | structure and phase analysis of calcium carbonate powder prepared by a simple solution method |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8593454/ https://www.ncbi.nlm.nih.gov/pubmed/34816040 http://dx.doi.org/10.1016/j.heliyon.2021.e08344 |
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