Your browser doesn't support javascript.
loading
Hydroxymethylfurfural as an Intermediate of Cellulose Carbonization.
Nomura, Takashi; Minami, Eiji; Kawamoto, Haruo.
Afiliación
  • Nomura T; Graduate school of Energy Science, Kyoto University Yoshida-honmachi Sakyo-ku, Kyoto, 606-8501, Japan.
  • Minami E; Graduate school of Energy Science, Kyoto University Yoshida-honmachi Sakyo-ku, Kyoto, 606-8501, Japan.
  • Kawamoto H; Graduate school of Energy Science, Kyoto University Yoshida-honmachi Sakyo-ku, Kyoto, 606-8501, Japan.
ChemistryOpen ; 10(6): 610-617, 2021 06.
Article en En | MEDLINE | ID: mdl-33931955
Hydrogen bond donor solvents such as aromatic solvents inhibit the secondary degradation of cellulose-derived primary pyrolysis products. In a previous study, we found that the formation of solid carbonized products was completely inhibited during cellulose pyrolysis in aromatic solvents, with 5-hydroxymethylfurfural (5-HMF) recovered in certain yields instead. This indicated that 5-HMF is an intermediate in cellulose carbonization. To confirm this hypothesis, the thermal reactivity of 5-HMF was investigated. At 280 °C, pure 5-HMF polymerized into a hard glassy substance through OH group elimination, but further conversion was slow. When pyrolyzed in the presence of glycerol, a model of coexisting primary pyrolysis products from cellulose, a coupling reaction proceeded. Reactions characteristic of cellulose carbonization then occurred, including the formation of acidic groups and benzene-type structures in the solid products. These results confirmed the above hypothesis. The molecular mechanism of cellulose carbonization is discussed, focusing on the crystalline nature.
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: ChemistryOpen Año: 2021 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Alemania

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: ChemistryOpen Año: 2021 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Alemania