Construction of Macromolecules of Depolymerized Lignite.

ABSTRACT

Preparing ash-less coal and further converting it into chemicals is an efficient and promising means for lignite utilization. This work performed depolymerization of lignite to prepare ash-less coal (SDP) and separated it into the hexane-soluble fraction (HS), toluene-soluble fraction (TS), and tetrahydrofuran-soluble fraction (THFS). The structure of SDP and those of subfractions were characterized by elemental analysis, gel permeation chromatography, Fourier transform infrared spectroscopy, and synchronous fluorescence spectroscopy. The results show that SDP is a mixture of aromatic derivatives containing alkyl substituents and oxygen-containing functional groups. The number of condensed aromatic rings, the amount of oxygen-containing functional groups, and the molecular weight gradually increase as HS < TS < THFS. SDP was further analyzed by 1H-NMR and 13C-NMR to calculate its structural parameters. The macromolecule of THFS contains 15.8 total ring systems with 9.2 aromatic rings and 6.6 naphthenic rings. On average, each THFS molecule contains 6.1 alcohol hydroxyl groups, 3.9 phenol hydroxyl groups, 1.4 carboxyl groups, and 1.0 inactive oxygen-containing functional groups. The dominant reactions occurred during depolymerization are the breakage of ether linkages. The average THFS molecule consists of 3.3 structural units with aromatic nuclei (2.8 rings on average) linked with methylene, naphthene, and so forth.