Mechanism study on the interaction between holocellulose and lignin during secondary pyrolysis of biomass: In terms of molecular model compounds

木质素 愈创木酚 热解 丁香酚 化学 异丁醇 糠醛 单体 呋喃 烷氧基 有机化学 聚合物 烷基 催化作用
作者
Han Zhang,Ming Liu,Yang Yang,Wei Chen,Jinjiao Zhu,Shihong Zhang,Haiping Yang,Hanping Chen,Yingquan Chen
出处
期刊:Fuel Processing Technology [Elsevier BV]
卷期号:244: 107701-107701 被引量:12
标识
DOI:10.1016/j.fuproc.2023.107701
摘要

A thorough examination of the interaction between holocellulose and lignin during secondary pyrolysis of biomass is essential for the targeted management of pyrolysis products. In this work, the interaction between holocellulose and lignin model compounds was explored utilizing a self-designed micro-pyrolysis device with a U-tube reactor. The content and distribution of liquid/gaseous products were investigated to determine potential interaction reaction routes. Holocellulose-lignin interaction was discovered to enhance the formation of furan products from the ring-opened C5/C6 monomer while blocking its conversion to anhydrous pyranose. The homolysis of methoxy groups on lignin model compounds is important for their interaction with holocellulose. Although phenol is generally stable, the phenolic hydroxyl group boosts the activity of the holocellulose monomer. The holocellulose monomer significantly promotes the cracking of the branched chains of guaiacol and syringol while inhibiting eugenol cleavage. Furfural induces eugenol condensation, resulting in the formation of dimers such as naphthalene and naphthalenol. The interaction between holocellulose monomer and eugenol primarily enhances the carboxylation of eugenol vinyl groups to generate aromatic acid compounds. The finding improves knowledge of the interactions that occur during secondary pyrolysis of biomass.

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