解聚
催化作用
木质素
双金属片
化学
氢氧化物
X射线光电子能谱
单体
有机化学
无机化学
聚合物
化学工程
工程类
作者
Gayan Karunasinghe,Dali Qian,Mark S. Meier,Mark Crocker,Michela Martinelli
标识
DOI:10.1002/slct.202401532
摘要
Abstract Lignin, a phenolic‐rich biomass component, holds promise for producing value‐added products. However, its complex structure and recalcitrance present challenges for its effective utilization. To overcome this, a AuPd/Li−Al layered double hydroxide (LDH) catalyst was developed to facilitate lignin depolymerization. Various AuPd bimetallic nanoparticle compositions were supported on a basic Li−Al LDH support via a sol‐immobilization method and characterized using N 2 ‐physisorption, X‐ray photoelectron spectroscopy (XPS), and transmission electron microscopy (TEM). The catalysts were then evaluated in the oxidation of several benzylic alcohols using O 2 as the oxidant, from which Au 7 Pd 3 /Li−Al LDH and Au 1 Pd 1 /Li−Al LDH were identified as possessing promising catalytic activity. Further investigations focused on the aerobic oxidation of β‐O‐4 linked lignin model dimers under atmospheric pressure. The tested catalysts demonstrated sequential oxidation of the model compounds, leading to cleavage of the β‐O‐4 linkage. Finally, the catalysts were applied to the oxidative deconstruction of γ‐valerolactone (GVL) extracted maple lignin at 120 °C. Au 1 Pd 1 /Li−Al LDH emerged as the most effective catalyst, yielding a range of aromatic monomers with a total monomer yield of 27 %. These results highlight the potential of the Au 1 Pd 1 /Li−Al LDH catalyst system as an eco‐friendly approach for lignin depolymerization under mild conditions.
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