期刊
CHEMICAL ENGINEERING & TECHNOLOGY
卷 44, 期 11, 页码 2126-2138出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/ceat.202100239
关键词
Alkyl substitution; Esterification; Hydrodeoxygenation; Model bio-oil; Ni2P; HZSM-5 catalyst
资金
- China Scholarship Council (CSC)
- GenComm Interreg project
Hydrodeoxygenation of model bio-oils, including acetic acid, phenol, acetone, 4-ethylguaiacol, furfural, and water, was performed using Ni2P/HZSM-5 catalysts. The conversion rate of acetic acid increased with temperature, in contrast to phenol due to differential adsorption capacity. Acetone was formed by self-ketonization of acetic acid, and different reaction networks were proposed for the main reactions.
Hydrodeoxygenation (HDO) of Mixture 1 (acetic acid and phenol) and Mixture 2 (acetone, acetic acid, phenol, 4-ethylguaiacolis, furfural, and water) as model bio-oils was performed to investigate the interactions. Ni2P/HZSM-5 catalysts exhibited higher activity than blank HZSM-5. The conversion rate of acetic acid enhanced with the increase of temperature, contrary to the value of phenol due to the differential adsorption capacity on active phases. Acetone can be formed by self-ketonization of acetic acid. Low temperatures favored esterification, while high temperatures promoted the synthesis of alkyl-substituted phenols and aromatic hydrocarbons via mainly alkyl substitution of phenol and benzene, respectively. Two reaction networks of model bio-oil HDO with the main reactions were proposed.
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