Ti incorporation in MCM-41 mesoporous molecular sieves using hydrothermal synthesis

2014 ◽  
Vol 8 (1) ◽  
pp. 95-103 ◽  
Author(s):  
Shengping Wang ◽  
Changqing Ma ◽  
Yun Shi ◽  
Xinbin Ma
2010 ◽  
Vol 1279 ◽  
Author(s):  
Yajie Guo ◽  
Guangjian Wang ◽  
Yuran Wang ◽  
Zhengwang Li ◽  
Guangqing Liu ◽  
...  

AbstractMesoporous molecular sieves MCM-41 modified by single (Ti) and bimetal (Ti-V) ions with highly ordered hexagonal arrangement of their cylindrical channels were prepared by direct synthesis under microwave–hydrothermal (M–H) conditions at 403K. Characterizations with powder X-ray diffraction (XRD), 29Si magic-angle spinning (MAS) NMR, N2 adsorption–desorption, Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), X-ray photoelcctron spectra(XPS) and transmission electron microscopy (TEM) showed that Ti and V ions were introduced into MCM-41 under M-H conditions and Ti/V-Si bond was formed. Results revealed that all the samples were of a typical hexagonal arrangement of mesoporous structure. The modified materials were high active and selective in the epoxidation of styrene at 343 K in comparison with single-functional MCM-41. Moreover, compared to conventional method, the presented microwave hydrothermal synthesis of molecular sieves greatly improved the selectivity to styrene oxide, e.g., it reached 58.6% at styrene conversion of 18.7% over Ti-V-MCM-41 (50).


1999 ◽  
Vol 35 (1) ◽  
pp. 52-56
Author(s):  
F. M. Bobonich ◽  
Yu. G. Voloshina ◽  
L. A. Matkovskaya ◽  
V. N. Solomakha ◽  
Yu. G. Gol’tsov

2011 ◽  
Vol 7 ◽  
pp. 22-28 ◽  
Author(s):  
Hynek Balcar ◽  
Tushar Shinde ◽  
Naděžda Žilková ◽  
Zdeněk Bastl

A commercially available Hoveyda–Grubbs type catalyst (RC303 Zhannan Pharma) was immobilized on mesoporous molecular sieves MCM-41 and on SBA-15 by direct interaction with the sieve wall surface. The immobilized catalysts exhibited high activity and nearly 100% selectivity in several types of alkene metathesis reactions. Ru leaching was found to depend on the substrate and solvent used (the lowest leaching was found for ring-closing metathesis of 1,7-octadiene in cyclohexane – 0.04% of catalyst Ru content). Results of XPS, UV–vis and NMR spectroscopy showed that at least 76% of the Ru content was bound to the support surface non-covalently and could be removed from the catalyst by washing with THF.


2001 ◽  
Vol 171 (1-2) ◽  
pp. 229-241 ◽  
Author(s):  
Rodica Tismaneanu ◽  
Biswajit Ray ◽  
Rafael Khalfin ◽  
Rafi Semiat ◽  
Moris S. Eisen

ChemInform ◽  
2000 ◽  
Vol 31 (41) ◽  
pp. no-no
Author(s):  
M. Ziolek ◽  
I. Nowak ◽  
I. Sobczak ◽  
A. Lewandowska ◽  
P. Decyk ◽  
...  

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