Abstract

Unsupported nano-phase MoS 2, CoS, and CoS-MoS 2 (Mo/Co mole ratio ∼6/1) materials were prepared in hexadecane by sonolysis of the corresponding metal carbonyls at ∼50 °C in high (>90%) yields as measured by the evolved carbon monoxide. Direct sonolysis of commercial micron-sized MoS 2 in hexadecane did not result in nano-sizing. The TEM images showed that the synthesized MoS 2 were aggregates of ∼20 nm mean particle diameter, CoS was ∼50 nm and the mixed-metal CoS-MoS 2 could be viewed as a composite in which smaller MoS 2 particles resided on the larger crystallites of CoS. The broad XRD peaks were consistent with nano-structured MoS 2 and the sharp peaks were consistent with a more crystalline CoS-MoS 2 species. The sharp peaks did not fit any single CoS pattern suggesting multiple phases. The XRD data showed that sonolysis did not alter the morphology of the micron-sized commercial MoS 2 sample. In the HDS comparative activity study of dibenzothiophene, the synthesized nano-phase MoS 2 exhibited more than an order of magnitude higher activity than its commercial micron-sized counterpart and the addition of Co further enhanced the activity. The HDS activity mirrored the temperature programmed reduction data. Interestingly, the nano-phase materials were less active for hydrogenation of 1-octene during the HDS study.

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