Preparation of nanocrystalline titania powder via aerosol pyrolysis of titanium tetrabutoxide
Source abstract
Abstract
Nanocrystalline titanium dioxide was prepared via aerosol pyrolysis of titanium alkoxide precursor at 200–580 °C in air and in nitrogen atmospheres. Powders were characterized by x-ray diffraction, thermogravimetric analysis, Brunauer–Emmett–Teller analysis, scanning electron microscopy, transmission electron microscopy, energy dispersive spectroscopy, x-ray fluorescence, Raman and infrared spectroscopy, and Berner-type low-pressure impactor. The anatase phase transition was initiated at 500 °C in nitrogen and at 580 °C in air. Under other conditions amorphous powders were observed and transformed to nanocrystalline TiO2 via thermal postannealing. In air, smooth and spherical particles with 2–4-μm diameter were formed with an as-expected tendency to convert to rutile in the thermal postannealings. In nitrogen, a fraction of the titanium tetrabutoxide precursor evaporated and formed ultrafine particles via the gas-to-particle conversion. At 500 °C thermally stable anatase phase was formed in nitrogen. A specific surface area as high as 280 m2 g−1 was observed for an as-prepared powder.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: TiO2 Photocatalysis and Solar Cells · Catalytic Processes in Materials Science · Advanced Photocatalysis Techniques
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (51)
Show source-provided references
1. 10.1016/0021-9797(79)90285-610.1016/0021-9797(79)90285-6 ↗
2. 10.1038/358048a010.1038/358048a0 ↗
3. 10.1111/j.1151-2916.1992.tb04442.x10.1111/j.1151-2916.1992.tb04442.x ↗
4. 10.1111/j.1151-2916.1965.tb14774.x10.1111/j.1151-2916.1965.tb14774.x ↗
5. 10.2109/jcersj1950.93.1079_38210.2109/jcersj1950.93.1079_382 ↗
6. Levine · 1975
7. 10.1002/aic.69043131610.1002/aic.690431316 ↗
8. 10.1557/JMR.1994.210210.1557/JMR.1994.2102 ↗
9. 10.1016/0040-6090(81)90362-X10.1016/0040-6090(81)90362-X ↗
10. 10.1016/0009-2509(89)85010-910.1016/0009-2509(89)85010-9 ↗
11. 10.1002/aic.69032121110.1002/aic.690321211 ↗
12. Bekkerman · Russ. J. Inorg. Chem. · 1976 · 21 · 223
13. 10.1063/1.10427410.1063/1.104274 ↗
14. 10.1016/0025-5408(70)90123-610.1016/0025-5408(70)90123-6 ↗
15. 10.1557/JMR.1993.233610.1557/JMR.1993.2336 ↗
16. Kroschwitz · 1997 · 24 · 235
17. 10.1016/0040-6090(92)90794-C10.1016/0040-6090(92)90794-C ↗
18. 10.1111/j.1151-2916.1967.tb15013.x10.1111/j.1151-2916.1967.tb15013.x ↗
19. 10.1007/BF0111739910.1007/BF01117399 ↗
20. 10.1080/0278682970896549810.1080/02786829708965498 ↗
21. 10.1111/j.1151-2916.1988.tb05852.x10.1111/j.1151-2916.1988.tb05852.x ↗
22. 10.1016/S0965-9773(96)00050-510.1016/S0965-9773(96)00050-5 ↗
23. 10.1021/cm00021a00310.1021/cm00021a003 ↗
24. 10.1364/AO.21.00296010.1364/AO.21.002960 ↗
25. 10.1557/JMR.1994.124110.1557/JMR.1994.1241 ↗
26. Ollis · Environ. Sci. Technol. · 1991 · 5 · 1523
27. 10.1080/0278682930895965010.1080/02786829308959650 ↗
28. 10.1007/BF0111739910.1007/BF01117399 ↗
29. 10.1007/BF0036075410.1007/BF00360754 ↗
30. 10.1007/BF0027444910.1007/BF00274449 ↗
31. 10.1111/j.1151-2916.1993.tb04007.x10.1111/j.1151-2916.1993.tb04007.x ↗
32. 10.1016/0021-9797(83)90091-710.1016/0021-9797(83)90091-7 ↗
33. 10.1016/0021-9797(84)90406-510.1016/0021-9797(84)90406-5 ↗
34. 10.1016/0021-8502(88)90026-210.1016/0021-8502(88)90026-2 ↗
35. 10.1039/a700301c10.1039/a700301c ↗
36. Langlet · 1992 · 55
37. Lide · 1997
38. 10.1121/1.190902010.1121/1.1909020 ↗
39. 10.1038/309319a010.1038/309319a0 ↗
40. 10.1080/0278682910895946910.1080/02786829108959469 ↗
41. West · 1984
42. Ahonen · 1998 · 1 · 205
43. 10.1080/1478643690822870610.1080/14786436908228706 ↗
44. Brinker · 1990
45. 10.1351/pac19855704060310.1351/pac198557040603 ↗
46. Bailar · 1973
47. 10.1007/BF0040269410.1007/BF00402694 ↗
48. 10.1007/BF0027534310.1007/BF00275343 ↗
49. MacKenzie · Trans. J. Br. Ceram. Soc. · 1975 · 74 · 29
50. MacKenzie · Trans. J. Br. Ceram. Soc. · 1975 · 74 · 121
51. 10.1023/A:101857950069110.1023/A:1018579500691 ↗