journal article·2011-07

Nonionic emulsion-mediated synthesis of zeolite beta

Yuguo Shen, Ying Zhang, Chao Jin, Ying Cao, Wei Gao, Lishan Cui

Bulletin of Materials Science· Volume 34· Issue 4
Publisher page

Abstract

Zeolite beta synthesis was first carried out in a newly developed emulsion system containing nonionic polyoxyethylated alkylphenol surfactant, which showed interesting non-conventional features. Compared to the conventional hydrothermal synthesis of zeolite beta, the reported nonionic emulsion system showed a faster nucleation rate. Furthermore, the emulsion system could stabilize the beta product and retarded its further transformation to ZSM-5 even under the high crystallization temperature at 453 K. Additionally, the beta particle size could be tuned by the adoption of different lengths of alkyl chain in the surfactant and cosurfactant. Control experiments showed each emulsion component played a crucial role in the zeolite beta growth. The approach proposed in this paper might be extended to apply for the syntheses of other types of zeolites with particle size under control.
Source: openaire · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Zeolite Catalysis and Synthesis · Mesoporous Materials and Catalysis · Catalysis and Hydrodesulfurization Studies

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

References (16)

Show source-provided references
1. Camblor M A, Barrett P A, Díaz-Cabañas M J, Villaescusa L A, Puche M, Boix T, Pérez E and Koller H 2001 Micropor. Mesopor. Mater. 48 1110.1016/S1387-1811(01)00325-0 ↗
2. Camblor M A, Corma A and Valencia S. 1996 Chem. Commun. 236510.1039/cc9960002365 ↗
3. Camblor M A, Mifsud A and Perez-Pariente J 1991 Zeolites 11 79210.1016/S0144-2449(05)80057-0 ↗
4. Carr C S and Shantz D F 2005 Micropor. Mesopor. Mater. 85 28410.1016/j.micromeso.2005.06.029 ↗
5. Cundy C S and Cox P A 2005 Micropor. Mesopor. Mater. 82 110.1016/j.micromeso.2005.02.016 ↗
6. Hari Prasad Rao P R, Ueyama K and Matsukata M 1998 Appl. Catal. A166 9710.1016/S0926-860X(98)80005-7 ↗
7. Jin C, Zhang Y, Gao W and Cui L S 2010 Int. J. Mod. Phys. B24 323610.1142/S0217979210066380 ↗
8. Kong L, Chen H, Tai J, Shen J, Zhang S and Chen J 2009 Mater. Lett. 63 34310.1016/j.matlet.2008.10.042 ↗
9. Lee S and Shantz D F. 2004 Chem. Comm. 68010.1039/b315646j ↗
10. Lee S and Shantz D F. 2005a Chem. Mater. 17 40910.1021/cm0486114 ↗
11. Lee S and Shantz D F. 2005b Micropor. Mesopor Mater. 86 26810.1016/j.micromeso.2005.07.026 ↗
12. Liu Z, Ohsuna T, Terasaki O and Camblor M A 2001 J. Am. Chem. Soc. 123 537010.1021/ja0107778 ↗
13. Matsukata M, Osaki T, Ogura M and Kikuchi E. 2002 Micropor. Mesopor. Mater. 56 110.1016/S1387-1811(02)00412-2 ↗
14. Modhera B, Chakraborty M, Parikh P A and Jasra R V 2009 Cryst. Res. Technol. 44 37910.1002/crat.200800474 ↗
15. Sun J, Zhu G, Chen Y, Li J, Wang L, Peng Y and Qiu S 2007 Micropor. Mesopor. Mater. 102 24210.1016/j.micromeso.2006.12.050 ↗
16. Wadlinger R L, Kerr G T and Rosinski E J 1967 U.S. Patent 3308069