Abstract

Mesityl oxide is standardly used to produce methyl iso butyl ketone but it can be also used to produce other useful compounds. Three catalysts were used for the reaction of the mesityl oxide reduction. They were NiW, NiMo, and CoMo supported on phonolite modified by HCl (metals/Ph-HCl). The fresh catalysts were characterized by XRD, XRF, BET surface, Hg porosimetry, SEM, H2-TPR, NH3-TPD, CO2-TPD. The materials were directly used, previously reduced in H2 or sulfided for the mesityl oxide reduction under H2 atmosphere. The reaction was performed in an autoclave at T = 375 °C, p = 50 bar (H2), and TOS = 1.5 h. The products were analyzed by GC/MS, GC/FID-TCD, ATR. The main products were methyl isobutyl ketone, 2-methyl pentane, and 2-methyl-2-pentene. Sulfided metal catalysts were the most active in the methyl isobutyl ketone, where the NiWSx/Ph-HCl catalyst showed the highest activity. For the non-previously-activated and hydrogen activated catalysts the most active catalyst was the NiMo/Ph-HCl for the production of methyl isobutyl ketone. The catalyst CoMo/Ph-HCl activated in hydrogen was the most active for the production of 2-methyl pentane compared to the other two hydrogen-activated materials.

Highlights

  • Mesityl oxide (MSO) can be obtained from acetone by aldol condensation reaction producing diacetone alcohol (DAA)

  • The Mo content in the catalysts with NiMo and CoMo was much higher than expected using a similar method of impregnation compared to the impregnation of Ni and W

  • The phonolite catalysts were active in the MSO reduction

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Summary

Introduction

Mesityl oxide (MSO) can be obtained from acetone by aldol condensation reaction producing diacetone alcohol (DAA). MSO can be used as solvent for phenol-formaldehyde resins, in PVC compounds and urea derivatives as feed for cattle, sheep, and poultry [1]. It can be used in general as a solvent for synthetic fibers and rubbers, oils, gums, resins, lacquers, varnishes, inks, stains, and insect repellent [2]. Acetone is produced by the cumene hydroperoxide process. It can be produced by dehydrogenation of 2-propanol (isopropyl alcohol) [3,4,5]

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