Ethanolysis of lignite is an effective approach for converting
organic matter of lignite to liquid coal derivatives. Xilinguole lignite
(XL) was reacted with ethanol at 320 °C. Then ethanol and isometric
carbon disulfide/acetone mixture were used to extract the reaction
mixture in a modified Soxhlet extractor to afford extractable portion
1 (EP1) and extractable portion 2 (EP2), respectively.
According to analysis of EP1 with a gas chromatography/mass
spectrometer, phenolic compounds made up more than 33% of the compounds
detected. This could be ascribed to the ethanolysis of XL; that is,
ethanol could selectively break the Calkyl–O bonds
in lignite, producing more phenolic compounds. Furthermore, a quadrupole
Orbitrap mass spectrometer equipped with an atmospheric pressure chemical
ionization source was used for comprehensive analysis of the compositional
features of EP1. The analysis indicated that O1–3, N1O0–2, and N2S1O3–6 were predominant class species in EP1. Nitrogen atoms in NO-containing organic compounds may exist in
the form of pyridine or amidogen, while oxygen atoms primarily exist
in furan, alkoxy, carbonyl, and ester groups. In addition, possible
chemical structures of NO-containing organic compounds were speculated.