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- W4286209463 abstract "The conversion of lignin into value-added chemicals is one of the important ways for sustainable development. Herein, phytic acid, a biomass-derived chemical, was used as the phosphorus source and pore former to synthesize the AlPyOx support. After loading Ni, the Ni/AlPyOx catalysts were found to be highly active in the catalytic conversion of lignin model compounds to high-value-added chemicals under mild conditions. The benzyl phenyl ether (α-O-4 lignin model compound) could be completely converted into toluene and phenol with near-equivalent selectivity at 30 °C and 3 MPa H2. Diphenyl ether and 2-phenoxy-1-phenylethanol were also used as 4-O-5 and β-O-4 model compounds of lignin, respectively. The unique activity of Ni/AlP0.5Ox could be attributed to metallic Ni that interacts with AlP0.5Ox and the unique adsorption of substrates on the carrier. Lignin can also be degraded over Ni/AlP0.5Ox via selective cleavage of the C–O bond, and 26.60 wt % yield of identified monomers was obtained." @default.
- W4286209463 created "2022-07-21" @default.
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- W4286209463 date "2022-07-20" @default.
- W4286209463 modified "2023-10-14" @default.
- W4286209463 title "Catalytic Cleavage of the C–O Bond in Lignin and Lignin-Derived Aryl Ethers over Ni/AlP<i><sub>y</sub></i>O<i><sub>x</sub></i> Catalysts" @default.
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- W4286209463 doi "https://doi.org/10.1021/acscatal.2c01523" @default.
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