Synthesis and characterization of mesoporous Si-MCM-41 materials and their application as solid acid catalysts in some esterification reactions
Source abstract
Abstract
Mesoporous MCM-41 has been synthesized by sol–gel method at room temperature possessing good thermal stability, high surface area as well as retention of surface area at high temperature. The MCM-41 neutral framework has been modified and put to practical use by incorporating Al3+ in the siliceous MCM-41 framework and supporting 12-TPA (12-tungstophosphoric acid) onto MCM-41 by process of anchoring and calcination to induce Bronsted acidity in MCM-41 to yield Al-MCM-41 and 12TPA-MCM-41, respectively. The synthesized materials have been characterized for elemental analysis by ICP-AES, XRD, SEM, TEM, EDX, FT–IR and TGA. Surface area has been determined by BET method and pore size and pore size distribution determined by BJH method. Surface acidity has been evaluated by NH3-TPD method. The potential use of Al-MCM-41 and 12TPA-MCM-41 as solid acid catalysts has been explored and compared by studying esterification as a model reaction wherein monoesters such as ethyl acetate (EA), propyl acetate (PA), butyl acetate (BA) and benzyl acetate (BzA) have been synthesized, optimizing several parameters such as catalyst amount, reaction time, reaction temperature and mole ratio of reagents.
Source: openaire · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Mesoporous Materials and Catalysis · Polyoxometalates: Synthesis and Applications · Zeolite Catalysis and Synthesis
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (17)
Show source-provided references
1. Aziz A Said A El, Abd El Wahab M M M and Alian A M 2007 J. Chem. Tech. Biotechnol. 82 51310.1002/jctb.1704 ↗
2. Beck J S, Kresge C T, Leonowicz M E, Roth W J and Vartuli J C 1992 Nature 359 71010.1038/359710a0 ↗
3. Dong S, Zhu M and Dai B 2012 Green Sust. Chem. 2 810.4236/gsc.2012.21002 ↗
4. Edler K J and White J W 1997 Chem. Mater. 9 122610.1021/cm9606033 ↗
5. Helen L N, Nicholas A, Zafiropoulos, Thomas F A, Edward T, Samulski D and Wenbin L 2010 J. Am. Oil Chem. Soc. 87 44510.1007/s11746-009-1509-x ↗
6. Jermy B R and Pandurangan A 2005 Appl. Catal. A: Gen. 295 18510.1016/j.apcata.2005.08.018 ↗
7. Juan J C, Zhang J and Yarmo M A 2007 J. Mol. Cat. 267 26510.1016/j.molcata.2006.09.029 ↗
8. Kozhevnikov V I, Sinnema A, Jansen R J, Pamin K and Van Bekkum H 1995 Catal. Lett. 30 24110.1007/BF00813690 ↗
9. Ma Y, Jin T, Wang Z and Li T 2003 Indian J. Chem. 42B 1777
10. Ma Y, Wang Q L, Jian W and Zuo B 1997 Appl. Catal. A: Gen. 165 19910.1016/S0926-860X(97)00201-9 ↗
11. Nascimento L A S, Tito L M Z, Angelina R S, Costa C E F, Zamian J R and Rocha G N 2011 Appl. Catal. B: Environ. 101 49510.1016/j.apcatb.2010.10.021 ↗
12. Otera J 2003 Esterification—Methods, reactions and applications (Weinheim, Germany: Wiley-VCH GmbH & Co. KGaA)10.1002/3527601848 ↗
13. Sharath K R, Vijayshree S and Nagaraju N 2001 Indian J. Chem. Tech. 8 362
14. Srilatha K, Kumar R, Prabhavathi Devi B L A, Prasad R B N, Sai Prasada P S and Lingaiah N 2011 Catal. Sci. Technol. 1 66210.1039/c1cy00085c ↗
15. Xia Q H, Hidajat K and Kawi S 2000 Mater. Lett. 42 10210.1016/S0167-577X(99)00167-6 ↗
16. Yadav G and Murkute A D 2003 Int. J. Chem. Reactor Eng. 1 110.2202/1542-6580.1126 ↗
17. Zhao Z H 2001 J. Mol. Catal. 168 14710.1016/S1381-1169(00)00515-X ↗