摘要
Depolymerizing lignin to prepare aromatic high-value chemicals is beneficial to solve the problem of energy shortage and waste of resources. However, cleavage of lignin C C bonds still faces greater challenges due to the recalcitrance of C C bonds in lignin. Photocatalysis is considered to be a promising way to break lignin C C bonds under mild conditions. Here, the micellar aqueous medium (SDS) composed of sodium lauryl sulfonate and water was prepared. 1, 2-Diphenylethanol (lignin model compound, Dpol) and dioxanesolv poplar lignin can be well dispersed in SDS-8 (mass fraction of 0.08% for sodium lauryl sulfate). Photocatalyst g-C 3 N 4 can efficiently break the lignin C C bonds in SDS-8 and very high photocatalytic efficiency can be obtained. A small amount of acetic acid can further improve photocatalytic efficiency. The main products produced by photocatalytic breaking lignin C C bonds are benzaldehyde and benzoic acid. The mechanism of photocatalytic cleavage of lignin C C bonds mainly follows a photogenerated electron-hole coupled redox mechanism. Thereinto, the hydrogen provided by SDS-8 has powerfully promoted photocatalytic efficiency. Our work provides a new direction for photocatalytic cleavage of lignin C C bonds into aromatic high-value chemicals.
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