A template-free method for the synthesis of porous alumina with superhigh specific surface area and large pore volume
This work demonstrates a facile organic-free and template-free approach for synthesizing spindle-like alumina with large pore volume and high specific surface area via a gas-liquid interfacial method followed by calcination. The influences of different calcination temperatures on the porous alumina...
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Veröffentlicht in: | Microporous and mesoporous materials 2020-01, Vol.292, p.109752, Article 109752 |
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Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | This work demonstrates a facile organic-free and template-free approach for synthesizing spindle-like alumina with large pore volume and high specific surface area via a gas-liquid interfacial method followed by calcination. The influences of different calcination temperatures on the porous alumina were systematically studied. The possible formation mechanism of the spindle-like structures was also investigated. The results exhibited that the as-obtained amorphous alumina calcined at 300 °C had superhigh surface areas (up to 853 m2/g). Furthermore, the adsorption performance of the as-prepared amorphous alumina with high surface area was also evaluated. This spindle-like amorphous alumina showed an excellent adsorption capacity (3284 mg/g) for the removal of Congo red from aqueous solution, which indicate this porous alumina may have great potential applications in adsorption and other related areas.
Spindle-like porous alumina with superhigh specific surface area were successfully synthesized for wastewater treatment via a simple and mild gas-liquid interfacial method using cheap inorganic salts without any surfactant or organic template. [Display omitted]
•The porous alumina powders were synthesized by a simple gas-liquid contact method.•After calcination at 300 °C, the as-obtained alumina possess superhigh surface area (853 m2/g).•This superhigh-surface-area alumina powders presented excellent adsorption properties. |
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ISSN: | 1387-1811 1873-3093 |
DOI: | 10.1016/j.micromeso.2019.109752 |