Related Experiment Video
Updated: Sep 9, 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 Catalytic Depolymerization of Lignin to Targeted Phenolic Monomers Using Noble Metals Supported on MgAl2O4
Shukun Qiu1,2, Zhiping Wu1, Xudong Liu2
1College of Materials and Energy, Central South University of Forestry and Technology, Changsha 410004, China.
None:
Reductive catalytic depolymerization of lignin to obtain value-added phenolic monomers has great potential. However, achieving the efficient depolymerization of lignin under hydrogen-free conditions while selectively obtaining specific monomers remains a significant challenge. In this study, MgAl2O4-based catalysts with well-developed pore structures and abundant oxygen vacancies were fabricated, exhibiting excellent catalytic performance in the depolymerization of various kinds of biomass. Importantly, a 39.0 wt % yield of phenolic monomers under hydrogen-free conditions over 5 wt % Pd/MgAl2O4 was comparable to that obtained under a H2 atmosphere from poplar. Furthermore, a high selectivity of 91.3% toward propanol-substituted monomers was obtained from pine. The efficient catalytic hydrogenolysis ability of the catalyst could be attributed to the highly dispersed small-sized metal nanoparticles, strong interaction between noble metal and MgAl2O4 support, and abundant medium-to-strong acidic sites. This study provides a green and efficient catalytic strategy for the valorization of lignin, contributing to the fabrication of phenolic monomers with high selectivity.
Related Concept Videos
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...
Radical Oxidation of Allylic and Benzylic Alcohols
Acid Halides to Alcohols: LiAlH4 Reduction
The mechanism proceeds in three steps. First, the nucleophilic hydride ion attacks the carbonyl carbon of the acid halide to form a tetrahedral intermediate. Next, the carbonyl group is re-formed, and the halide ion departs as a leaving group, generating an aldehyde. A second nucleophilic attack by the hydride yields an alkoxide ion, which, upon protonation, gives a primary alcohol as...
Oxidation of Alkenes: Syn Dihydroxylation with Potassium Permanganate
Reduction of Alkynes to cis-Alkenes: Catalytic Hydrogenation
Like alkenes, alkynes can be reduced to alkanes in the presence of transition metal catalysts such as Pt, Pd, or Ni. The reaction involves two sequential syn additions of hydrogen via a cis-alkene intermediate.
Oxidation of Alkenes: Syn Dihydroxylation with Osmium Tetraoxide

