Journal
FUEL
Volume 223, Issue -, Pages 222-229Publisher
ELSEVIER SCI LTD
DOI: 10.1016/j.fuel.2018.03.014
Keywords
Temperature-controlled hydrogenation; Condensed arenes; Polycyclic alkanes; Hydroarenes
Categories
Funding
- Fundamental Research Funds for the Central Universities [2017BSCXB26]
- Postgraduate Research & Practice Innovation Program of Jiangsu Province [KYCX17_1506]
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Catalyst Ni/attapulgite powder (AP) was facilely prepared by thermally decomposing nickel tetracarbonyl onto AP. Anthracene was used as a condensed arenes (CAs)-related model compound to evaluate the catalytic activity and selectivity of Ni/AP for hydrogenating CAs. The results show that anthracene can be completely converted to perhydroanthracenes (PHAs) at 175 degrees C and selectively converted to 9,10-dihydroanthracene (DHA, ca. 86.4%) at 300 degrees C by catalytic hydrogenation over Ni/AP. Ni/AP effectively promotes the formation and transfer (F & T) of biatomic active hydrogen (H center dot center dot center dot H) at 175 degrees C, resulting in the complete hydrogenation of anthracene to PHAs. The mechanism for the F & T of H center dot center dot center dot H is consistent with the observation from the higher selectivities of cis-PHAs than that of trans-PHAs. At 300 degrees C, the catalytically produced H center dot center dot center dot H over Ni/AP tends to be homolytically spitted to hydrogen radical (H-center dot), inducing the partial hydrogenation of anthracene to DHA. Quantum chemical calculations based on density functional theory further confirmed the temperature-controlled hydrogenation of anthracene over Ni/AP. This finding is a conclusive proof that the active hydrogen species is crucially important for affecting the product selectivities from the catalytic hydrogenation of anthracene over Ni/AP. Our research also offers a novel strategy for highly selective conversion of CAs to polycyclic alkanes or hydroarenes.
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