摘要
Lignin, due to its structural rigidity, tends to form coke deposits during catalytic hydrodeoxygenation (HDO), causing catalyst deactivation, and eliminating coke to restore performance is challenging. In this study, Co 3 O 4 shows excellent HDO performance toward lignin model dimers with high selectivity for demethoxylation and deethoxylation under mild conditions via a one-step strategy integrating in-situ reduction and HDO, and enables lignin HDO. At 240 o C, 2 MPa, and 20 h, lignin achieved a 73 % liquid yield, with 64%, 30%, and 6% selectivities to alkanes, alcohols, and phenols. This is attributed to Co 3 O 4 's high Co-O bond energy, dominant (220) crystal plane exposure, and high Co 3+ /Co 2+ ratio, facilitating in-situ reduction to metallic cobalt active sites. Coke on Co 3 O 4 can be removed by calcination to restore performance, with 90% of the initial liquid yield retained after five cycles. This low-cost commercial non-noble metal Co 3 O 4 enhances the economic feasibility of lignin's high-value utilization.IntroductionLignin, accounting for 15-30 wt% of lignocellulose, is the most abundant renewable aromatic resource on earth, holding immense potential to replace fossil feedstocks in producing high-value
危险品化学品经营许可证(带存储)