[article]
Titre : |
Facile sodium alginate assisted assembly of ni−al layered double hydroxide nanostructures |
Type de document : |
texte imprimé |
Auteurs : |
Hui Wang, Auteur ; Guoli Fan, Auteur ; Chen Zheng, Auteur |
Année de publication : |
2010 |
Article en page(s) : |
pp. 2759–2767 |
Note générale : |
Industrial Chemistry |
Langues : |
Anglais (eng) |
Mots-clés : |
Facile Sodium Alginate Assembly Layered Double Hydroxide Nanostructures |
Résumé : |
Self-assembled three-dimensional Ni−Al layered double hydroxide (LDH) nanostructures have been successfully synthesized using a facile biopolymer-assisted approach in the presence of a simple, safe, and inexpensive sodium alginate biopolymer under hydrothermal conditions. The structure and morphology of LDH nanostructures obtained have been investigated by scanning electron microscopy (SEM), powder X-ray diffraction (XRD), high-resolution transmission electron microscopy (HRTEM), Fourier transform infrared spectroscopy (FT-IR), thermogravimetric and differential thermal analysis (TG-DTA), and UV−visible diffuse spectroscopy (UV−vis). Three types of pompon-like, marigold-like, and coral-like LDH nanostructures could be obtained by adjusting the synthesis parameters including hydrothermal aging time, concentration of metal ions, and reaction temperature. A possible formation mechanism for the controlled organization of primary LDH nanosheet building units into special three-dimensional nanostructures is proposed on the basis of the interaction between sodium alginate molecules and LDH crystals. Furthermore, after calcination of LDHs at 500 and 700 °C, the resulting NiO-based mixed metal oxides still maintain the three-dimensional morphology of their LDH precursors to some extent, indicative of the high thermal stability of nanostructures. The findings in this work provide a feasible approach for the morphosynthesis of LDH nanomaterials with special superstructures. |
Note de contenu : |
Bibiogr. |
ISSN : |
0888-5885 |
En ligne : |
http://pubs.acs.org/doi/abs/10.1021/ie901519h |
in Industrial & engineering chemistry research > Vol. 49 N° 6 (Mars 2010) . - pp. 2759–2767
[article] Facile sodium alginate assisted assembly of ni−al layered double hydroxide nanostructures [texte imprimé] / Hui Wang, Auteur ; Guoli Fan, Auteur ; Chen Zheng, Auteur . - 2010 . - pp. 2759–2767. Industrial Chemistry Langues : Anglais ( eng) in Industrial & engineering chemistry research > Vol. 49 N° 6 (Mars 2010) . - pp. 2759–2767
Mots-clés : |
Facile Sodium Alginate Assembly Layered Double Hydroxide Nanostructures |
Résumé : |
Self-assembled three-dimensional Ni−Al layered double hydroxide (LDH) nanostructures have been successfully synthesized using a facile biopolymer-assisted approach in the presence of a simple, safe, and inexpensive sodium alginate biopolymer under hydrothermal conditions. The structure and morphology of LDH nanostructures obtained have been investigated by scanning electron microscopy (SEM), powder X-ray diffraction (XRD), high-resolution transmission electron microscopy (HRTEM), Fourier transform infrared spectroscopy (FT-IR), thermogravimetric and differential thermal analysis (TG-DTA), and UV−visible diffuse spectroscopy (UV−vis). Three types of pompon-like, marigold-like, and coral-like LDH nanostructures could be obtained by adjusting the synthesis parameters including hydrothermal aging time, concentration of metal ions, and reaction temperature. A possible formation mechanism for the controlled organization of primary LDH nanosheet building units into special three-dimensional nanostructures is proposed on the basis of the interaction between sodium alginate molecules and LDH crystals. Furthermore, after calcination of LDHs at 500 and 700 °C, the resulting NiO-based mixed metal oxides still maintain the three-dimensional morphology of their LDH precursors to some extent, indicative of the high thermal stability of nanostructures. The findings in this work provide a feasible approach for the morphosynthesis of LDH nanomaterials with special superstructures. |
Note de contenu : |
Bibiogr. |
ISSN : |
0888-5885 |
En ligne : |
http://pubs.acs.org/doi/abs/10.1021/ie901519h |
|