Journal
APPLIED ENERGY
Volume 332, Issue -, Pages -Publisher
ELSEVIER SCI LTD
DOI: 10.1016/j.apenergy.2022.120489
Keywords
Kraft lignin; Biochar; Bifunctional catalyst; Aqueous-phase glycerol medium; Guaiacol; ?-O-4 model substance
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This study reports a catalytic process using microporous biochar (BC) derived from lignin supported Ni-Ce catalysts for the depolymerization of lignin to guaiacol and 4-alkyl guaiacols in an aqueous-phase glycerol medium. The catalytic system showed high yields of the target compounds due to the promotion of metallic Ni sites and the interaction of Ni with CeO2, which resulted in the formation of Ni-CeO2-x interfaces and oxygen vacancies that could adsorb and activate the bonds of lignin and its fragments.
Developing an advanced catalytic system for the purposeful depolymerization of lignin into aromatic compounds has presented a significant prospect for green manufacturing. In this paper, the catalytic process of microporous biochar (BC) derived from lignin supported Ni-Ce catalysts (xNi-Ce/BC) coupling with the aqueous-phase glycerol medium was reported for the depolymerization of Kraft lignin to guaiacol and 4-alkyl guaiacols. Under the optimal conditions, 3Ni-Ce/BC yielded 59.02 % of lignin oil and simultaneously realized the highest yields of guaiacol (243.94 mg/g lignin) and 4-alkyl guaiacols (265.65 mg/g lignin). The characterization results revealed BC promoted the formation of metallic Ni sites and the interaction of Ni with CeO2 drove the generation of Ni-CeO2-x interfaces and oxygen vacancies (OV). These could adsorb and activate the C-C and C-O bonds of lignin and its depolymerized fragments to form reactive intermediates. Then, the Ni sites activated the aqueous -phase glycerol to form adsorbed H atoms, which then spilled over to the adjacent OV to stabilize reactive in-termediates. Subsequently, the optimal distribution between Bronsted acid sites (BAS) and Lewis acid sites (LAS) in 3Ni-Ce/BC enhanced the yields of guaiacol and 4-alkyl guaiacols. The kinetic analysis adopting 2-phenoxy-1-phenylethanol as the beta-O-4 bond model demonstrated that 3Ni-Ce/BC significantly reduced both the bond dissociation energy of beta-O-4 bond and the apparent activation energy. Finally, the possible reaction mechanism
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