催化作用
八面体
材料科学
布朗斯特德-洛瑞酸碱理论
活动中心
木质素
化学计量学
单体
选择性
尖晶石
结晶学
路易斯酸
化学
无机化学
冶金
晶体结构
聚合物
有机化学
复合材料
作者
Yi Qi,Xin Xiao,Yuqing Mei,Lingyingzi Xiong,Liheng Chen,Xuliang Lin,Zhan Lin,Shirong Sun,Bing Han,Dongjie Yang,Yanlin Qin,Xueqing Qiu
标识
DOI:10.1002/adfm.202111615
摘要
Abstract Rational design and construction of catalysts with regulable active sites for selective cleavage of lignin to produce aromatic monomers remain challenging. Herein, the authors report a new strategy for tuning the active sites of tetrahedral centers (Lewis acid sites) and octahedral centers (Brønsted acid sites) in Ni x Co 3− x O 4 through tailoring the non‐stoichiometric ratio of Ni and Co. The ratio of Ni and Co is experimentally optimized for the optimal acidic activity of catalytic cracking of lignin when x = 0.2. The Ni 0.2 Co 2.8 O 4 catalysts achieve an outstanding catalytic conversion (up to 81 wt%) for the lignin cleavage and excellent selective cleavage into aromatic monomers (up to 90.30 wt%), which is mainly attributed to the optimized electron rearrangement, adjustable active sites, and synergistic effect between these two active sites. This work provides a new concept to rationally design solid acid catalysts for the efficient conversion of lignin.
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