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Formation of Soluble Furanic and Carbocyclic Oxy-Organics during the Hydrothermal Carbonization of Glucose
journal contribution
posted on 2020-01-14, 14:07 authored by Ning Shi, Qiying Liu, Ying Liu, Lijun Chen, Ni Chen, Jiayu Peng, Longlong MaIn this study, the
water-soluble products formed during the hydrothermal
carbonization of glucose were analyzed by liquid chromatography (LC)–mass
spectrometry (MS) and LC–MS2 to determine the formulas
and the possible structures of the main compounds. In addition to
the well-known compounds of 3-deoxyglucosone, 5-hydroxymethylfurfural,
and levulinic acid, the furanic compounds and the carbocyclic oxy-organics
containing hydroxy group and carbonyl group with a molecular mass
range between 170 and 260 Da were also identified. Both C–C
coupling reaction and C–C cleavage reaction were proved to
be involved during the formation of these carbocyclic oxy-organics,
so they were proposed to be released via C–C cleavage of the
primary polymers, which were formed by aldol condensation of the primary
precursors formed during the degradation of glucose. The identification
of these carbocyclic oxy-organics was indirect evidence that aldol
condensation played a crucial role during the formation of hydrochar
from carbonization of glucose.