Abstract

Co3O4/MCM-41 adsorbents were successfully prepared by ultrasonic assisted impregnation (UAI) and traditional mechanical stirring impregnation (TMI) technologies and characterized by X-ray diffraction (XRD), N2 adsorption desorption, Fourier transform infrared spectra (FT-IR), transmission electron microscopy (TEM), scanning electron microscopy (SEM) and thermogravimetry-differential thermal analysis (TG-DTA). The H2S removal performances for a simulated low H2S concentration gas were investigated in a fixed-bed. The effect of preparation and adsorption conditions on the H2S removal over Co3O4/MCM-41 were systematically examined. The results showed that UAI promotes more and well defined highly dispersed active Co3O4 phase on MCM-41. As compared to the Co3O4/MCM-41-T prepared via TMI, the saturated H2S capacity of Co3O4/MCM-41-U prepared via UAI improved by 33.2%. The desulfurization performance of adsorbents decreased in the order of Co3O4/MCM-41-U > Co3O4/MCM-41-T > MCM-41. The Co3O4/MCM-41-U prepared using Co(NO3)2 concentration of 10%, ultrasonic time of 2 h, calcination temperature of 550 °C and calcination time of 3 h exhibited the best H2S removal efficiency. At adsorption temperature of 25 °C with model gas flowrate of 20 mL min−1, the breakthrough time of Co3O4/MCM-41-U was 10 min, and the saturated H2S capacity and H2S removal rate was 52.6 mg g−1 and 47.8%, respectively.

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