Ambient-pressure and low-temperature upgrading of lignin bio-oil to hydrocarbons using a hydrogen buffer catalytic system

加氢脱氧 除氧 化学 催化作用 有机化学 碳氢化合物 选择性
作者
Wei Liu,Wenqin You,Wei Sun,Weisheng Yang,Akshay Korde,Yutao Gong,Yulin Deng
出处
期刊:Nature Energy [Nature Portfolio]
卷期号:5 (10): 759-767 被引量:143
标识
DOI:10.1038/s41560-020-00680-x
摘要

Catalytic hydrodeoxygenation is an essential step for bio-oil upgrading. However, hydrodeoxygenation usually requires a high hydrogen pressure and high temperature due to the good stability of the C–O bonds. Here we report an effective multiphase hydrodeoxygenation of lignin-based bio-oil at temperatures <100 °C and hydrogen pressures <1 atm using a synergetic catalyst system that consists of a low redox potential H4SiW12O40 (SiW12) and suspended Pt-on-carbon (Pt/C) particles. We propose that SiW12 plays three critical roles in bio-oil hydrodeoxygenation. First, it quickly oxidizes the H2 gas to form reduced SiW12 in the presence of Pt/C. Second, it transfers both electrons and H+ ions to the bulk phase to form active H* or H2 on the Pt/C surface. Third, the formation of the oxonium ion in a SiW12 superacid solution reduces the deoxygenation energy. The SiW12-enhanced proton-transfer hydrodeoxygenation mechanism is supported by density functional theory computations. As a result of the hydrogen buffer and acidic effect, up to a 90% yield of hydrocarbons (cyclohexane, benzene and their derivatives) was achieved from the hydrodeoxygenation of phenol and its derivatives. Bio-oil derived from biomass has great potential as a more sustainable fuel but its formation typically relies on energy-intensive processes. Liu et al. show how a tri-phase hydrogen-transfer catalytic system can drive hydrodeoxygenation in water under mild conditions to achieve up to 90% hydrocarbon yield.
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