Fabrication and characterization of titania inverse opals using supercritical carbon dioxide
[Display omitted] ► Titania inverse opals (TIO) synthesis by using scCO2 investigated. ► Colloidal PS particle was used as a template, titanium tetra-isopropoxide (TTIP), ethanol and water acted as infiltrating reaction materials. ► After the sol–gel coating reaction and subsequent thermal treatment...
Gespeichert in:
Veröffentlicht in: | The Journal of supercritical fluids 2012-07, Vol.67, p.71-75 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | [Display omitted]
► Titania inverse opals (TIO) synthesis by using scCO2 investigated. ► Colloidal PS particle was used as a template, titanium tetra-isopropoxide (TTIP), ethanol and water acted as infiltrating reaction materials. ► After the sol–gel coating reaction and subsequent thermal treatment, TIO structure obtained. ► The synthesized TIO have anatase crystalline structure and have mean pore size diameter of 670–700nm showing only 2–5% shrinkage from the original PS latex spheres (715nm).
Titania inverse opals (TIO) with macropores were synthesized via hydrolysis of titanium tetra-isopropoxide (TTIP) in supercritical carbon dioxide (scCO2). Colloidal polystyrene (PS) particles packed in a regular arrangement were used as a template. A mixture of scCO2, TTIP along with ethanol (EtOH) and distilled water was used as an impregnation medium to the voids of PS template. After the sol–gel coating reaction of the titania precursor in the voids and a subsequent thermal treatment, an inverted titania opal structure with high periodicity was obtained. The TIO was characterized by field emission scanning electron microscopy (FE-SEM), Raman spectroscopy and X-ray diffractometry (XRD). From the results of analysis, we conclude that the TIO synthesized in this study have anatase crystalline structure and have mean pore size diameter of 670–700nm. The change in particle sizes is equivalent to only 2–5% shrinkage from the original PS latex spheres (715nm). This represents much improved result compared to the products made by other methods where 20–30% shrinkage is common. |
---|---|
ISSN: | 0896-8446 1872-8162 |
DOI: | 10.1016/j.supflu.2012.03.005 |