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Experimental Investigation and Simplistic Geochemical Modeling of CO(2) Mineral Carbonation Using the Mount Tawai Peridotite
In this work, the potential of CO(2) mineral carbonation of brucite (Mg(OH)(2)) derived from the Mount Tawai peridotite (forsterite based (Mg)(2)SiO(4)) to produce thermodynamically stable magnesium carbonate (MgCO(3)) was evaluated. The effect of three main factors (reaction temperature, particle s...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6273465/ https://www.ncbi.nlm.nih.gov/pubmed/26999082 http://dx.doi.org/10.3390/molecules21030353 |
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author | Rahmani, Omeid Highfield, James Junin, Radzuan Tyrer, Mark Pour, Amin Beiranvand |
author_facet | Rahmani, Omeid Highfield, James Junin, Radzuan Tyrer, Mark Pour, Amin Beiranvand |
author_sort | Rahmani, Omeid |
collection | PubMed |
description | In this work, the potential of CO(2) mineral carbonation of brucite (Mg(OH)(2)) derived from the Mount Tawai peridotite (forsterite based (Mg)(2)SiO(4)) to produce thermodynamically stable magnesium carbonate (MgCO(3)) was evaluated. The effect of three main factors (reaction temperature, particle size, and water vapor) were investigated in a sequence of experiments consisting of aqueous acid leaching, evaporation to dryness of the slurry mass, and then gas-solid carbonation under pressurized CO(2). The maximum amount of Mg converted to MgCO(3) is ~99%, which occurred at temperatures between 150 and 175 °C. It was also found that the reduction of particle size range from >200 to <75 µm enhanced the leaching rate significantly. In addition, the results showed the essential role of water vapor in promoting effective carbonation. By increasing water vapor concentration from 5 to 10 vol %, the mineral carbonation rate increased by 30%. This work has also numerically modeled the process by which CO(2) gas may be sequestered, by reaction with forsterite in the presence of moisture. In both experimental analysis and geochemical modeling, the results showed that the reaction is favored and of high yield; going almost to completion (within about one year) with the bulk of the carbon partitioning into magnesite and that very little remains in solution. |
format | Online Article Text |
id | pubmed-6273465 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62734652018-12-28 Experimental Investigation and Simplistic Geochemical Modeling of CO(2) Mineral Carbonation Using the Mount Tawai Peridotite Rahmani, Omeid Highfield, James Junin, Radzuan Tyrer, Mark Pour, Amin Beiranvand Molecules Article In this work, the potential of CO(2) mineral carbonation of brucite (Mg(OH)(2)) derived from the Mount Tawai peridotite (forsterite based (Mg)(2)SiO(4)) to produce thermodynamically stable magnesium carbonate (MgCO(3)) was evaluated. The effect of three main factors (reaction temperature, particle size, and water vapor) were investigated in a sequence of experiments consisting of aqueous acid leaching, evaporation to dryness of the slurry mass, and then gas-solid carbonation under pressurized CO(2). The maximum amount of Mg converted to MgCO(3) is ~99%, which occurred at temperatures between 150 and 175 °C. It was also found that the reduction of particle size range from >200 to <75 µm enhanced the leaching rate significantly. In addition, the results showed the essential role of water vapor in promoting effective carbonation. By increasing water vapor concentration from 5 to 10 vol %, the mineral carbonation rate increased by 30%. This work has also numerically modeled the process by which CO(2) gas may be sequestered, by reaction with forsterite in the presence of moisture. In both experimental analysis and geochemical modeling, the results showed that the reaction is favored and of high yield; going almost to completion (within about one year) with the bulk of the carbon partitioning into magnesite and that very little remains in solution. MDPI 2016-03-16 /pmc/articles/PMC6273465/ /pubmed/26999082 http://dx.doi.org/10.3390/molecules21030353 Text en © 2016 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons by Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Rahmani, Omeid Highfield, James Junin, Radzuan Tyrer, Mark Pour, Amin Beiranvand Experimental Investigation and Simplistic Geochemical Modeling of CO(2) Mineral Carbonation Using the Mount Tawai Peridotite |
title | Experimental Investigation and Simplistic Geochemical Modeling of CO(2) Mineral Carbonation Using the Mount Tawai Peridotite |
title_full | Experimental Investigation and Simplistic Geochemical Modeling of CO(2) Mineral Carbonation Using the Mount Tawai Peridotite |
title_fullStr | Experimental Investigation and Simplistic Geochemical Modeling of CO(2) Mineral Carbonation Using the Mount Tawai Peridotite |
title_full_unstemmed | Experimental Investigation and Simplistic Geochemical Modeling of CO(2) Mineral Carbonation Using the Mount Tawai Peridotite |
title_short | Experimental Investigation and Simplistic Geochemical Modeling of CO(2) Mineral Carbonation Using the Mount Tawai Peridotite |
title_sort | experimental investigation and simplistic geochemical modeling of co(2) mineral carbonation using the mount tawai peridotite |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6273465/ https://www.ncbi.nlm.nih.gov/pubmed/26999082 http://dx.doi.org/10.3390/molecules21030353 |
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