| Summary: | The present work concerns the preparation of SAPO-11 materials using microwave (MW) heating during the crystallization process. Different experimental conditions such as crystallization temperature and time were explored, together with different Si sources. The final materials were fully characterized using chemical analysis, XRD diffraction, pyridine adsorption followed by FTIR, nitrogen sorption and NMR spectroscopy and compared with the respective conventional SAPO-11 materials, synthesized using the same initial chemical composition of the gel but under conventional electric heating. The results showed that SAPO-11 materials can be synthesized in less time (within minutes) and at lower temperature (170 °C) with MW heating than with conventional heating (respectively 24 h and 200 °C). MW heating allows nanosized SAPO-11 materials to be obtained but the nature of the Si source used has a marked influence on the textural properties and, especially, on the acidity of SAPO-11. The catalytic properties of the materials (with 0.5 wt.% Pt) were evaluated in the hydroisomerization of long chain n-alkanes using n-decane as model molecule. Optimized MW samples using colloidal AS-40 Si source showed higher yields in monobranched isomers due to a joint effect of low acidity and suitable textural properties.
|
|---|