Por favor, use este identificador para citar o enlazar a este item:
http://hdl.handle.net/10261/188549
COMPARTIR / EXPORTAR:
SHARE CORE BASE | |
Visualizar otros formatos: MARC | Dublin Core | RDF | ORE | MODS | METS | DIDL | DATACITE | |
Título: | Lithium-based sorbents for high temperature CO2 capture: Effect of precursor materials and synthesis method |
Autor: | Izquierdo Pantoja, María Teresa CSIC ORCID ; Gasquet, V.; Sansom, E.; Ojeda, Manuel; García, S.; Maroto Valer, Mercedes | Palabras clave: | CO2 capture Li-based sorbents Fly ash Rietveld refinement |
Fecha de publicación: | 12-may-2018 | Editor: | Elsevier | Citación: | Fuel 230: 45-51 (2018) | Resumen: | The aim of this work was to study the effect of the silica source (pure reagent or fly ash, FA) and preparation method (solid state reaction and precipitation method) using Li-pure reagents on the CO2 uptake at high temperature of the prepared sorbents. CO2 uptake of sorbents prepared from pure reagents or FA was compared. A relationship between surface area, pore volume and particle size with CO2 uptake of the prepared samples was not found. X-ray diffraction (XRD) characterization revealed different Li4SiO4 contents in the produced samples. Sample prepared from Li2CO3 and SiO2 pure reagents by solid state method had a high Li4SiO4 content (91.5 wt%), but in the presence of FA the main compound was Li2CaSiO4, which has a low theoretical CO2 uptake capacity. There is a negligible effect of the preparation method on samples prepared from LiOH with either pure silica or FA. However, for pure reagents (LiOH and SiO2), the Li4SiO4 content was lower than that found when Li2CO3 was used as starting material, probably due to a lower synthesis temperature. For LiOH-FA derived samples, XRD patterns showed that CaO was the main crystal phase and the Li content was low, indicating that this element was probably present in the amorphous phase. Except for the Li4SiO4 rich sample, a linear relationship was found between the experimentally measured CO2 uptake and the theoretically calculated one based on the stoichiometry of carbonation reactions exhibited by active phases contained within each sorbent, and normalised to crystal phase contents. Despite the high CaO content in some of the FA-derived samples, the carbonation reaction does not proceed via CaCO3 formation and Li2CaSiO4 and Ca5(SiO4)2CO3 crystal phases are present in the carbonated samples, limiting the CO2 capture of CaO present in the fly ash. | Descripción: | 5 Figures, 4 Tables.-- © 2018. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/ | Versión del editor: | http://dx.doi.org/10.1016/j.fuel.2018.05.041 | URI: | http://hdl.handle.net/10261/188549 | DOI: | 10.1016/j.fuel.2018.05.041 | ISSN: | 0016-2361 |
Aparece en las colecciones: | (ICB) Artículos |
Ficheros en este ítem:
Fichero | Descripción | Tamaño | Formato | |
---|---|---|---|---|
FUEL_Lithium-based sorbents_2018.pdf | Artículo principal | 915,4 kB | Adobe PDF | Visualizar/Abrir |
CORE Recommender
SCOPUSTM
Citations
40
checked on 04-abr-2024
WEB OF SCIENCETM
Citations
36
checked on 24-feb-2024
Page view(s)
219
checked on 18-abr-2024
Download(s)
262
checked on 18-abr-2024
Google ScholarTM
Check
Altmetric
Altmetric
Este item está licenciado bajo una Licencia Creative Commons