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Synthesis of highly stable metal-containing extra-large-pore molecular sieves
Author(s) -
Raquel MartínezFranco,
Cecilia Paris,
Manuel Moliner,
Avelino Corma
Publication year - 2016
Publication title -
philosophical transactions of the royal society a mathematical physical and engineering sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.074
H-Index - 169
eISSN - 1471-2962
pISSN - 1364-503X
DOI - 10.1098/rsta.2015.0075
Subject(s) - molecular sieve , zeolite , fourier transform infrared spectroscopy , catalysis , molecule , metal , infrared spectroscopy , materials science , desorption , spectroscopy , scanning electron microscope , inorganic chemistry , chemical engineering , chemistry , adsorption , organic chemistry , physics , quantum mechanics , engineering , composite material
The isomorphic substitution of two different metals (Mg and Co) within the framework of the ITQ-51 zeotype (IFO structure) using bulky aromatic proton sponges as organic structure-directing agents (OSDAs) has allowed the synthesis of different stable metal-containing extra-large-pore zeotypes with high pore accessibility and acidity. These metal-containing extra-large-pore zeolites, named MgITQ-51 and CoITQ-51, have been characterized by different techniques, such as powder X-ray diffraction, scanning electron microscopy, energy dispersive X-ray spectrometry, UV-Vis spectroscopy, temperature programmed desorption of ammonia and Fourier transform infrared spectroscopy, to study their physico-chemical properties. The characterization confirms the preferential insertion of Mg and Co atoms within the crystalline structure of the ITQ-51 zeotype, providing high Brønsted acidity, and allowing their use as efficient heterogeneous acid catalysts in industrially relevant reactions involving bulky organic molecules.

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