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Interaction of Pristine Hydrocalumite-Like Layered Double Hydroxides with Carbon Dioxide

[Image: see text] The layered double hydroxides (LDHs) of Ca(2+) and trivalent cations, Al(3+) and Fe(3+), are single-source precursors to generate supported CaO, which picks up CO(2) from the gas phase in the temperature range 350–550 °C. The supports are ternary oxides, mayenite, and Ca(2)Fe(2)O(5...

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Autores principales: Narayanappa, Anand N., Kamath, P. Vishnu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2019
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6648629/
https://www.ncbi.nlm.nih.gov/pubmed/31459537
http://dx.doi.org/10.1021/acsomega.9b00083
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author Narayanappa, Anand N.
Kamath, P. Vishnu
author_facet Narayanappa, Anand N.
Kamath, P. Vishnu
author_sort Narayanappa, Anand N.
collection PubMed
description [Image: see text] The layered double hydroxides (LDHs) of Ca(2+) and trivalent cations, Al(3+) and Fe(3+), are single-source precursors to generate supported CaO, which picks up CO(2) from the gas phase in the temperature range 350–550 °C. The supports are ternary oxides, mayenite, and Ca(2)Fe(2)O(5). The uptake capacity of the Fe(3+)-containing LDH at 1.9 mmol g(–1) is two times the capacity of the Al(3+)-containing LDH. The product of CO(2) uptake is calcite CaCO(3). It is observed that the intercalated chloride ions reduce the thermal penalty by inducing the early decomposition of CaCO(3). In the case of the chloride-intercalated LDHs of Ca(2+) and Fe(3+), the CaCO(3) formed is completely decomposed at 900 °C. This is in contrast with the CaCO(3) formed from bare CaO, which shows no sign of decomposition at 900 °C under similar conditions. This work shows that the hydrocalumite-like LDHs are candidate materials for CO(2) mineralization.
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spelling pubmed-66486292019-08-27 Interaction of Pristine Hydrocalumite-Like Layered Double Hydroxides with Carbon Dioxide Narayanappa, Anand N. Kamath, P. Vishnu ACS Omega [Image: see text] The layered double hydroxides (LDHs) of Ca(2+) and trivalent cations, Al(3+) and Fe(3+), are single-source precursors to generate supported CaO, which picks up CO(2) from the gas phase in the temperature range 350–550 °C. The supports are ternary oxides, mayenite, and Ca(2)Fe(2)O(5). The uptake capacity of the Fe(3+)-containing LDH at 1.9 mmol g(–1) is two times the capacity of the Al(3+)-containing LDH. The product of CO(2) uptake is calcite CaCO(3). It is observed that the intercalated chloride ions reduce the thermal penalty by inducing the early decomposition of CaCO(3). In the case of the chloride-intercalated LDHs of Ca(2+) and Fe(3+), the CaCO(3) formed is completely decomposed at 900 °C. This is in contrast with the CaCO(3) formed from bare CaO, which shows no sign of decomposition at 900 °C under similar conditions. This work shows that the hydrocalumite-like LDHs are candidate materials for CO(2) mineralization. American Chemical Society 2019-02-13 /pmc/articles/PMC6648629/ /pubmed/31459537 http://dx.doi.org/10.1021/acsomega.9b00083 Text en Copyright © 2019 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Narayanappa, Anand N.
Kamath, P. Vishnu
Interaction of Pristine Hydrocalumite-Like Layered Double Hydroxides with Carbon Dioxide
title Interaction of Pristine Hydrocalumite-Like Layered Double Hydroxides with Carbon Dioxide
title_full Interaction of Pristine Hydrocalumite-Like Layered Double Hydroxides with Carbon Dioxide
title_fullStr Interaction of Pristine Hydrocalumite-Like Layered Double Hydroxides with Carbon Dioxide
title_full_unstemmed Interaction of Pristine Hydrocalumite-Like Layered Double Hydroxides with Carbon Dioxide
title_short Interaction of Pristine Hydrocalumite-Like Layered Double Hydroxides with Carbon Dioxide
title_sort interaction of pristine hydrocalumite-like layered double hydroxides with carbon dioxide
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6648629/
https://www.ncbi.nlm.nih.gov/pubmed/31459537
http://dx.doi.org/10.1021/acsomega.9b00083
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