High surface area sol–gel alumina–titania nanocatalyst
Source abstract
Abstract
Alumina–titania mixed oxide nanocatalysts with molar ratios = 1:0.5, 1:1, 1:2, 1:5 have been synthesized by adopting a hybrid sol–gel route using boehmite sol as the precursor for alumina and titanium isopropoxide as the precursor for titania. The thermal properties, XRD phase analysis, specific surface area, adsorption isotherms and pore size details along with temperature programmed desorption of ammonia are presented. A specific surface area as high as 291 m2/g is observed for 1:5 Al2O3/TiO2 composition calcined at 400 °C, but the same composition when calcined at 1,000 °C, resulted in a surface area of 4 m2/g, while 1:0.5 composition shows a specific surface area of 41 m2/g at 1,000 °C. Temperature programmed desorption (of ammonia) results show more acidic nature for the titania rich mixed oxide compositions. Transmission electron microscopy of low and high titania content samples calcined at 400 °C, shows homogeneous distribution of phases in the nano range. In the mixed oxide, the particle size ranges between 10–20 nm depending on titania content. The detailed porosity data analysis contributes very much in designing alumina–titania mixed oxide nanocatalysts.
Source: openaire · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Catalytic Processes in Materials Science · Zeolite Catalysis and Synthesis · Catalysis and Oxidation Reactions
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (13)
Show source-provided references
1. Colomban P (1987) Rev. Phys Appliquee 22:719. doi: 10.1051/rphysap:0198700220807190010.1051/rphysap:01987002208071900 ↗
2. Phachecomalagon G, Garucaborquez A, Costeer D, Sklyaroew A, Petit S, Fripiat JJ (1995) J Mater Res 10(5):1264. doi: 10.1557/JMR.1995.126410.1557/JMR.1995.1264 ↗
3. Kumar KNP, Keizer K, Burggraaf AJ (1993) J Mater Chem 3(9):917. doi: 10.1039/jm993030091710.1039/JM9930300917 ↗
4. Kumar KNP (1994) Appl. Catal. A. Gen 119(1):163. doi: 10.1016/0926-860X(94)85032-110.1016/0926-860X(94)85032-1 ↗
5. Ramirez J, Alejandre AG (1997) J Catal 170:108. doi: 10.1006/jcat.1997.171310.1006/jcat.1997.1713 ↗
6. Linacero R, Cervantes MLR, De L, Lopez-Gonzalez D (2000) J Mater Sci 35:3269. doi: 10.1023/A:100487532293510.1023/A:1004875322935 ↗
7. Lee HL, Lee HS (1994) J Mater Sci Lett 13:316. doi: 10.1007/BF0042078410.1007/BF00420784 ↗
8. Toba M, Mizukami F, Niwa S, Kiyozumi Y, Maeda K, Annila A, Komppa V (1994) J Mater Chem 4(4):585. doi: 10.1039/jm994040058510.1039/jm9940400585 ↗
9. Montoya JA, Delangel P, Viveros T (2001) J Mater Chem 11(3):944. doi: 10.1039/b008161m10.1039/b008161m ↗
10. Mani TV, Pillai PK, Damodaran AD, Warrier KGK (1994) Mater Lett 19:237. doi: 10.1016/0167-577X(94)90163-510.1016/0167-577X(94)90163-5 ↗
11. Lowel S, Shields JE (1984) Powder surface area and porosity, 2nd edn. Chapman and Hall, London10.1007/978-94-009-5562-2 ↗
12. Padmaja P, Krishna Pillai P, Warrier KGK, Padmanabhan M (2004) J Porous Mater 11:147. doi: 10.1023/B:JOPO.0000038010.54859.2f10.1023/B:JOPO.0000038010.54859.2f ↗
13. Padmaja P, Warrier KGK, Padmanabhan M, Wunderlich W, Berry FJ, Mortimer M, Creamer NJ (2006) Mater Chem Phys 95:56. doi: 10.1016/j.matchemphys.2005.05.04410.1016/j.matchemphys.2005.05.044 ↗