Related Experiment Video
Updated: Nov 26, 2025

Extraction of Lignin with High β-O-4 Content by Mild Ethanol Extraction and Its Effect on the Depolymerization Yield
Published on: January 7, 2019
Selective production of phenolic monomers via high efficient lignin depolymerization with a carbon based
Bochao Yan1, Xiaoyu Lin1, Zhihui Chen1
1Research Center for Biomass Energy, School of Resources and Environmental Engineering, East China University of Science and Technology, 130 Meilong Road, Shanghai 200237, China.
Abstract:
Lignin is an abundant renewable source of bio-aromatics and its valorization is of great importance. In this work, an efficient non-precious carbon based metal-Mo2C catalytic system for selective production of phenolic monomers (PMs) from organosolv lignin depolymerization is proposed. With the optimized catalyst of Ni-Fe-Mo2C, 89.56% of liquefaction and 35.53% of PMs yields were achieved under 260 ℃ for 4 h with water-methanol (4:1 v/v) solvent. Characterization of the catalysts shows that the induction of Ni-Fe species was favor for the formation of β-Mo2C, and efficiently promoted the lignin liquefaction. The decoration of Ni/Fe can also change the side chain hydrogenolysis ability of the catalyst and exhibite high yield for 4-ethylphenol (14.77%) production. Methanol, used as co-solvent, was found to play an important role in PMs production and lignin depolymerization. These results demonstrated that the Ni-Fe-Mo2C catalytic system has potential to produce valuable phenolic monomers from lignin under mild conditions.
Related Concept Videos
Alcohols from Carbonyl Compounds: Reduction
Catalytic hydrogenation is similar to the reduction of an alkene or alkyne by adding H2 across the pi bond in the presence of transition metal catalysts like Raney Ni, Pd–C, Pt, or Ru. Aldehydes and ketones can be reduced by this method, often under mild to moderate heat (25–100°C) and...
Catalysis
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...

