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dc.contributor.author
Salazar Hoyos, Luis Alfonso  
dc.contributor.author
Faroldi, Betina María Cecilia  
dc.contributor.author
Cornaglia, Laura Maria  
dc.date.available
2020-06-23T12:47:35Z  
dc.date.issued
2019-03  
dc.identifier.citation
Salazar Hoyos, Luis Alfonso; Faroldi, Betina María Cecilia; Cornaglia, Laura Maria; Reactivity of rice husk-derived lithium silicates followed by in situ Raman spectroscopy; Elsevier Science Sa; Journal of Alloys and Compounds; 778; 3-2019; 699-711  
dc.identifier.issn
0925-8388  
dc.identifier.uri
http://hdl.handle.net/11336/107890  
dc.description.abstract
Lithium silicates were synthesized using rice husk ash as a precursor of silica to be used in CO2 capture. Two different treatment steps, with water (SiO2-W) or HCl 3 M (SiO2-A), were carried out prior to the rice husk burning. Silica with a high surface area of 303 m2g-1, a yield of 16.9% and a purity of 96.8% was obtained for the acid treatment. Subsequently, silica was impregnated with LiNO3 employing different Li/Si molar ratios and two different methods, successive incipient wetness impregnation and wet impregnation. SEM images showed agglomerates of nanometric spheres (70?100 nm) for the silica, and polyhedral particles for the silicate samples. The presence of three silicate phases, Li2Si2O5, Li2SiO3, and Li4SiO4, with different proportions was found by XRD and Raman spectroscopy measurements. In addition, the effect of particle size, temperature and sorption time over the CO2 capture capacity was analyzed. The best performance was found in the Li/Si = 4.1-HW sample with a particle diameter of 0.3 mm and 2 h of isothermal capture at 863 K. In situ Raman experiments were carried out to follow the phase transformations during the capture/regeneration steps. All samples remained in a stable value of capture capacity after several sorption/desorption cycles.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
Elsevier Science Sa  
dc.rights
info:eu-repo/semantics/restrictedAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/  
dc.subject
CARBON DIOXIDE CAPTURE  
dc.subject
IN SITU RAMAN  
dc.subject
LITHIUM SILICATES  
dc.subject
RICE HUSKS  
dc.subject.classification
Ingeniería Química  
dc.subject.classification
Ingeniería Química  
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INGENIERÍAS Y TECNOLOGÍAS  
dc.title
Reactivity of rice husk-derived lithium silicates followed by in situ Raman spectroscopy  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2020-06-16T13:41:18Z  
dc.journal.volume
778  
dc.journal.pagination
699-711  
dc.journal.pais
Países Bajos  
dc.journal.ciudad
Amsterdam  
dc.description.fil
Fil: Salazar Hoyos, Luis Alfonso. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera"; Argentina  
dc.description.fil
Fil: Faroldi, Betina María Cecilia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera"; Argentina  
dc.description.fil
Fil: Cornaglia, Laura Maria. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera"; Argentina  
dc.journal.title
Journal of Alloys and Compounds  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S0925838818341537  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1016/j.jallcom.2018.11.036