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Coating-free TiO(2)@β-SiC alveolar foams as a ready-to-use composite photocatalyst with tunable adsorption properties for water treatment
Coating-free TiO(2)@β-SiC photocatalytic composite foams gathered within a ready-to-use shell/core alveolar medium the photocatalytically active TiO(2) phase and the β-SiC foam structure were prepared via a multi-step shape memory synthesis (SMS) replica method. They were fabricated following a sequ...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9048602/ https://www.ncbi.nlm.nih.gov/pubmed/35492643 http://dx.doi.org/10.1039/c9ra09553e |
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author | Rico-Santacruz, Marisa García-Muñoz, Patricia Marchal, Clément Batail, Nelly Pham, Charlotte Robert, Didier Keller, Nicolas |
author_facet | Rico-Santacruz, Marisa García-Muñoz, Patricia Marchal, Clément Batail, Nelly Pham, Charlotte Robert, Didier Keller, Nicolas |
author_sort | Rico-Santacruz, Marisa |
collection | PubMed |
description | Coating-free TiO(2)@β-SiC photocatalytic composite foams gathered within a ready-to-use shell/core alveolar medium the photocatalytically active TiO(2) phase and the β-SiC foam structure were prepared via a multi-step shape memory synthesis (SMS) replica method. They were fabricated following a sequential two-step carburization approach, in which an external TiC skin was synthesized at the surface of a β-SiC skeleton foam obtained from a pre-shaped polyurethane foam during a first carburization step. The adsorption behaviour of the shell/core TiO(2)@β-SiC composite foams towards the Diuron pollutant in water was tuned by submitting the carbide foams to a final calcination treatment within the 550–700 °C temperature range. The controlled calcination step allowed (i) the selective oxidation of the TiC shell into a TiO(2) crystallite shell owing to the β-SiC resistance to oxidation and (ii) the amount of residual unreacted carbon in the foams to be tuned. The lower the calcination temperature, the more pronounced the adsorption profiles of the composites and the higher the Diuron amount removed by adsorption on the residual unreacted carbon. The ready-to-use TiO(2)@β-SiC composite foams were active in the degradation of the Diuron pesticide, without any further post-synthesis immobilization or synthesis process at the foam surface. They displayed good reusability with test cycles and benefitted from an enhanced stability in terms of the titania release to water. |
format | Online Article Text |
id | pubmed-9048602 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90486022022-04-28 Coating-free TiO(2)@β-SiC alveolar foams as a ready-to-use composite photocatalyst with tunable adsorption properties for water treatment Rico-Santacruz, Marisa García-Muñoz, Patricia Marchal, Clément Batail, Nelly Pham, Charlotte Robert, Didier Keller, Nicolas RSC Adv Chemistry Coating-free TiO(2)@β-SiC photocatalytic composite foams gathered within a ready-to-use shell/core alveolar medium the photocatalytically active TiO(2) phase and the β-SiC foam structure were prepared via a multi-step shape memory synthesis (SMS) replica method. They were fabricated following a sequential two-step carburization approach, in which an external TiC skin was synthesized at the surface of a β-SiC skeleton foam obtained from a pre-shaped polyurethane foam during a first carburization step. The adsorption behaviour of the shell/core TiO(2)@β-SiC composite foams towards the Diuron pollutant in water was tuned by submitting the carbide foams to a final calcination treatment within the 550–700 °C temperature range. The controlled calcination step allowed (i) the selective oxidation of the TiC shell into a TiO(2) crystallite shell owing to the β-SiC resistance to oxidation and (ii) the amount of residual unreacted carbon in the foams to be tuned. The lower the calcination temperature, the more pronounced the adsorption profiles of the composites and the higher the Diuron amount removed by adsorption on the residual unreacted carbon. The ready-to-use TiO(2)@β-SiC composite foams were active in the degradation of the Diuron pesticide, without any further post-synthesis immobilization or synthesis process at the foam surface. They displayed good reusability with test cycles and benefitted from an enhanced stability in terms of the titania release to water. The Royal Society of Chemistry 2020-01-22 /pmc/articles/PMC9048602/ /pubmed/35492643 http://dx.doi.org/10.1039/c9ra09553e Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Rico-Santacruz, Marisa García-Muñoz, Patricia Marchal, Clément Batail, Nelly Pham, Charlotte Robert, Didier Keller, Nicolas Coating-free TiO(2)@β-SiC alveolar foams as a ready-to-use composite photocatalyst with tunable adsorption properties for water treatment |
title | Coating-free TiO(2)@β-SiC alveolar foams as a ready-to-use composite photocatalyst with tunable adsorption properties for water treatment |
title_full | Coating-free TiO(2)@β-SiC alveolar foams as a ready-to-use composite photocatalyst with tunable adsorption properties for water treatment |
title_fullStr | Coating-free TiO(2)@β-SiC alveolar foams as a ready-to-use composite photocatalyst with tunable adsorption properties for water treatment |
title_full_unstemmed | Coating-free TiO(2)@β-SiC alveolar foams as a ready-to-use composite photocatalyst with tunable adsorption properties for water treatment |
title_short | Coating-free TiO(2)@β-SiC alveolar foams as a ready-to-use composite photocatalyst with tunable adsorption properties for water treatment |
title_sort | coating-free tio(2)@β-sic alveolar foams as a ready-to-use composite photocatalyst with tunable adsorption properties for water treatment |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9048602/ https://www.ncbi.nlm.nih.gov/pubmed/35492643 http://dx.doi.org/10.1039/c9ra09553e |
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