Synthesis and Catalytic Applications of Novel Mesoporous Aluminosilicate Molecular Sieves

1996 ◽  
Vol 454 ◽  
Author(s):  
Kondam Madhusudan Reddy ◽  
Chunshan Song

ABSTRACTThis paper reports on the synthesis of four series of mesoporous aluminosilicate molecular sieves (Al-MCM-41) and their catalytic applications. Four different aluminum compounds were examined as Al source in the hydrothermal synthesis of the mesoporous aluminosilicates of MCM-41 type, including pseudo boehmite (alumina), aluminum sulfate, aluminum isopropoxide, and sodium aluminate. Each Al source was examined at three different feed Si/Al ratios in the synthesis. XRD results show that there are differences in the dioo-spacings for the samples prepared with different Al sources: sodium aluminate > Al isopropoxide > Al sulfate > pseudo boehmite. Such differences reveal that Al incorporation in the framework increases in the following order: pseudo boehmite < Al sulfate < Al isopropoxide < sodium aluminate. XRD also indicates that the synthesized Al-MCM-41 samples have different crystallinity. 27Al NMR and 29Si NMR reveal that most of the Al species in the samples prepared with pseudo boehmite were present in octahedral coordination, whereas in other samples nearly all the Al species are tetrahedral (in the framework). The acid characteristics of the synthesized molecular sieves were characterized by temperature-programmed desorption of n-butylamine, and by using 1,3,5-triisopropylbenzene hydrocracking as probe reaction. The results of TPD and probe reaction clearly indicate that the Al source used for synthesis has a major impact on the acidic and catalytic properties of Al-MCM-41. The samples prepared with Al isopropoxide and sodium aluminate are better as catalysts than those with Al sulfate and pseudo boehmite. We also explored the potential of mesoporous molecular sieves as support for noble metal hydrogenation catalysts and metal sulfide-based hydrotreating catalysts. Pd and Pt-loaded mesoporous molecular sieves were prepared and applied for hydrogenation of naphthalene and phenanthrene. The results show that mesoporous molecular sieve-supported catalysts are much more active than alumina- and titania-supported catalysts. The data for dibenzothiophene hydrodesulfurization suggest that Al-MCM-41 supported Co-Mo may be effective for deep desulfurization of distillate fuels.

1997 ◽  
Vol 50 (1) ◽  
pp. 53 ◽  
Author(s):  
Yau-Yan Lim ◽  
Dugald J. MacLachlan ◽  
Thomas D. Smith ◽  
Jim Jamis ◽  
John R. Pilbrow ◽  
...  

Infrared spectroscopic measurements have been made on hydrocarbons and hydrogen cyanide adsorbed, separately and competitively, on mesoporous molecular sieves MCM-41 of all-silica composition and with various aluminium(III) , titanium(IV) or vanadium(V) contents. Similar i.r. spectroscopic measurements were made on the porous aluminium phosphates AlPO4-5 and VPI. Characterization of the cationic binding sites of MCM-41 has been achieved by comparison of the e.s.r. spectra of the cationic copper(II) chelate acetylacetonatocopper(II) tetramethylethylenediamine, adsorbed by MCM-41, and by the sodium ion forms of zeolite-Y, mordenite, ultrastable and chromatographic grade silica. Both sets of results show that for mesoporous MCM-41 Brønsted acidity and possibly cation-exchange sites arise from ill-defined structural defects and from the silanol groups which are not greatly influenced by the presence of metal cations within the thick-walled honeycomb structure.


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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