Microwave-Induced One-Pot Preparation of Bifunctional N-Fe/BC Catalysts and Oriented Production of Phenol-Enriched Bio-Oil from Biomass Pyrolysis: Catalyst Synthesis, Performance Evaluation, and Mechanism Insight via Theoretical Calculations

被引:27
作者
Luo, Juan [2 ]
Gong, Guojin [1 ]
Cui, Chongwei [2 ]
Sun, Shichang [1 ]
Lin, Junhao [2 ]
Ma, Rui [1 ]
Sun, Jiaman [1 ]
机构
[1] Shenzhen Univ, Coll Chem & Environm Engn, Shenzhen 518060, Peoples R China
[2] Harbin Inst Technol, Sch Environm, Harbin 150090, Peoples R China
基金
中国国家自然科学基金;
关键词
microwave catalytic pyrolysis; bifunctional catalyst; phenol-enriched bio-oil; model compound; theoretical calculation; OXYGEN REDUCTION REACTION; CARBON MATERIALS; LIGNIN; HYDRODEOXYGENATION; NANOPARTICLES; ABSORPTION; GUAIACOL; ASH; TRANSFORMATION; KINETICS;
D O I
10.1021/acscatal.2c01841
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
To recover valuable products from biomass, bifunctional catalysts (N-Fe/BC) capable of microwave absorption and oriented production of phenolics were prepared by a one-pot method involving the microwave-induced K2FeO4. Its catalytic performances were evaluated, and the catalytic mechanism was explored using a model compound and DFT calculations. The cycle performance and deactivation mechanism were investigated. N-Fe/BC possessed a large S-BET value (265.21 m(2) g(-1)), good pore distribution, and abundant Fe and N species, resulting in good dielectric and catalytic properties. After catalysis, the heating rates reached 63.78-107.84 degrees C min(-1), and the selectivity and yield of phenol-enriched bio-oil improved significantly, reaching maximum values of 80.28% and 38.09 wt % at 550 degrees C with 20 wt % N-Fe/BC, respectively. Model compound experiments and DFT calculations showed that N-Fe/BC directionally generated phenolics by changing the reaction path and forming "hot spots" that stimulated the catalytic reforming of oxygen-containing compounds. The catalytic performance decreased slightly after five cycles, due to active site loss, carbon deposition, and pore collapse.
引用
收藏
页码:11318 / 11339
页数:22
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