Abstract

This study deals with the synthesis of catalytic samples containing MgO and 10, 15 and 25 wt% of CeO2 by co-precipitation method for aldol condensation of acetone. The obtained powders were characterized by X-ray diffraction (XRD), Raman spectroscopy, temperature programmed desorption of CO2, X-ray photoelectron spectroscopy, nitrogen physisorption, and atomic force microscopy. The materials exhibited XRD patterns corresponding with cubic MgO and fluorite phase of ceria, medium and weak strength basic sites, characteristic electronic properties and distinctive trends regarding textural properties. The aldol condensation of acetone was carried out using the prepared catalyst samples; a decrease in acetone conversion as function of time-on-stream was noted for all catalyst, being the best performance exhibited by the sample containing 10 wt% ceria. The selectivity toward the different products of aldol condensation of acetone was dependent on catalytic sample, which was related to the unique properties of those solids. Diacetone alcohol was best produced by MgO-25 wt% ceria; for mesityl oxide yield, an increase in selectivity as time-on-stream was observed being the best material the sample MgO-10wt% ceria; whereas for phorone, the profiles indicate almost yield reduction as time-on-stream function, indicating the best performance the sample containing 15 wt% of CeO2. Isophorone was optimally produced by using pure MgO which was attributed to the presence of medium strength basic sites and adequate textural properties.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.