Pore structure of aluminas derived from the alkyl derivatives of boehmite
Source abstract
Abstract
The alkyl derivatives of boehmite (alkoxyalumoxanes; AlO(OH)1−x (OR) x ) were synthesized by the reaction of aluminum triisopropoxide in straight-chain primary alcohols at 300 °C for 2 h in an autoclave. In the present work, pore structures of aluminas obtained by calcination of the alkyl derivatives of boehmite were examined. The alumina obtained from the ethyl derivative of boehmite had a broad pore-size distribution, while the pore-size of the alumina obtained from the dodecyl derivative of boehmite distributed in a narrow range in the mesopore region. The mode pore diameter of the latter alumina increased with the increase in calcination temperature (as-syn., 39 Å; 600 °C, 54 Å; 800 °C, 58 Å; 1000 °C, 68 Å), but narrow pore-size distribution was maintained even after calcination at high temperatures.
Source: expertdata · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Mesoporous Materials and Catalysis · Aerogels and thermal insulation · Advanced ceramic materials synthesis
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (22)
Show source-provided references
1. D.L. Trimm, A. Stanislaus, Appl. Catal. 21, 215 (1986). doi: 10.1016/S0166-9834(00)81356-110.1016/S0166-9834(00)81356-1 ↗
2. A.C. Pierre, E. Elaloui, G.M. Pajonk, Langmuir 14, 66 (1998). doi: 10.1021/la970044u10.1021/la970044u ↗
3. F. Vaudry, S. Khodabandeh, M.E. Davis, Chem. Mater. 8, 1451 (1996). doi: 10.1021/cm960033710.1021/cm9600337 ↗
4. S.A. Bagshaw, T.J. Pinnavaia, Angew. Chem. Int. Ed. Engl. 35, 1102 (1996). doi: 10.1002/anie.19961102110.1002/anie.199611021 ↗
5. W. Zhang, T.J. Pinnavaia, Chem. Commun. (Camb.) 1185 (1998). doi: 10.1039/a708178b10.1039/a708178b ↗
6. S. Valange, J.L. Guth, F. Kolenda, S. Lacombe, Z. Gabelica, Microporous Mesoporous Mater. 35–36, 597 (2000). doi: 10.1016/S1387-1811(99)00253-X10.1016/S1387-1811(99)00253-X ↗
7. X. Zhang, F. Zhang, K.Y. Chan, Mater. Lett. 58, 2872 (2004). doi: 10.1016/j.matlet.2004.05.00810.1016/j.matlet.2004.05.008 ↗
8. W.C. Li, A.H. Lu, W. Schmidt, F. Schüth, Chem. Eur. J. 11, 1658 (2005). doi: 10.1002/chem.20040077610.1002/chem.200400776 ↗
9. A. Ionescu, A. Allouche, J.P. Aycard, M. Rajzmann, F. Hutschka, J. Phys. Chem. B 106, 9359 (2002). doi: 10.1021/jp020145n10.1021/jp020145n ↗
10. M. Inoue, H. Kominami, T. Inui, J. Am. Ceram. Soc. 73, 1100 (1990). doi: 10.1111/j.1151-2916.1990.tb05164.x10.1111/j.1151-2916.1990.tb05164.x ↗
11. M. Inoue, M. Kimura, T. Inui, Chem. Mater. 12, 55 (2000). doi: 10.1021/cm990303w10.1021/cm990303w ↗
12. M. Inoue, Y. Kondo, T. Inui, Inorg. Chem. 27, 215 (1988). doi: 10.1021/ic00275a00110.1021/ic00275a001 ↗
13. M. Inoue, H. Tanino, Y. Kondo, T. Inui, Clays Clay Miner. 39, 151 (1991). doi: 10.1346/CCMN.1991.039020610.1346/CCMN.1991.0390206 ↗
14. J.J. Fripiat, H. Bosmans, P.G. Rouxhet, J. Phys. Chem. 71, 1097 (1967). doi: 10.1021/j100863a04810.1021/j100863a048 ↗
15. M.C. Stegmann, D. Vivien, C. Mazieres, Spectrichim. Acta. A 29A, 1653 (1973)10.1016/0584-8539(73)80115-1 ↗
16. A.B. Kiss, G. Keresztury, L. Farkas, Spectrochim. Acta. A Mol. Biomol. Spectrosc. 36A, 653 (1980)10.1016/0584-8539(80)80024-9 ↗
17. Y. Yacoub, R. Bata, M. Gautam, Proc. Instn. Mech. Eng. A 212, 363 (1998). doi: 10.1243/095765098153693410.1243/0957650981536934 ↗
18. Y. Nakazaki, M. Inoue, J. Phys. Chem. Solids 65, 429 (2004). doi: 10.1016/j.jpcs.2003.08.04310.1016/j.jpcs.2003.08.043 ↗
19. M. Kobayashi, S.-W. Kim, S. Iwamoto, M. Inoue, J. Phys. Chem. Solids 69, 1367 (2008). doi: 10.1016/j.jpcs.2007.10.08810.1016/j.jpcs.2007.10.088 ↗
20. J.H. de Boer, B.C. Lippens, J. Catal. 3, 38 (1964). doi: 10.1016/0021-9517(64)90090-910.1016/0021-9517(64)90090-9 ↗
21. B.C. Lippens, J.H. de Boer, J. Catal. 4, 319 (1965). doi: 10.1016/0021-9517(65)90307-610.1016/0021-9517(65)90307-6 ↗
22. T. Inui, T. Miyake, Y. Takegami, J. Jpn. Petrol. Inst. 25, 242 (1983)10.1627/jpi1958.25.242 ↗