A series of Mo-based catalysts for 1-butene metathesis to propene were prepared by supporting Mo species on SBA-15 premodified with alumina. The effects of the method of introduction of the alumina guest to the host SBA-15 on the location of the Mo species and the corresponding metathesis activity were studied. As revealed by N2 adsorption isotherms and TEM results, well-dispersed alumina was formed on the pore walls of SBA-15 if the ammonia/water vapor induced hydrolysis (NIH) method was employed. The Mo species preferentially interacted with alumina instead of SBA-15, as evidenced by X-ray photoelectron spectroscopy, time-of-flight secondary-ion mass spectrometry, and IR spectroscopy of adsorbed pyridine. Furthermore, new Brønsted acid sites favorable for the dispersion of the Mo species and low-temperature metathesis activity were generated as a result of the effective synergy between the alumina and SBA-15. The Mo/Al2O3@SBA-15 catalyst prepared by the NIH method showed higher metathesis activity and stability under the conditions of 120 °C, 0.1 MPa, and 1.5 h(-1) than catalysts prepared by other methods.
Keywords: alumina; metathesis; molybdenum; propene; sba-15.
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