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Environmental and economical concerns over diminishing landfill space and the growing abundance of mixed plastic waste mandate development of viable strategies for recovering high-valued resources from waste polymers. Co-processing of waste polymer mixtures with coal allows for the simultaneous conversion of coal and plastics into high-valued fuels. However, there is limited information about the underlying reaction pathways, kinetics, and mechanisms controlling coal liquefaction in the presence of polymeric materials. A series of model compound experiments has been conducted, providing a starting point for unraveling the complex, underlying chemistry. Neat pyrolysis studies of model compounds of polyethylene and coal were conducted in batch reactors. Tetradecane (C{sub 14} H{sub 30} ) was used as a polyethylene mimic, and 4-(naphthylmethyl)bibenzyl (NBBM) was used as a coal model compound. Reaction temperatures were 420 and 500 C, and batch reaction times ranged from 5--150 minutes. Detailed product analysis using gas chromatography and mass spectrometry enabled the reactant conversion and product selectivities to be determined. Reaction of single components and binary mixtures allowed the kinetic coupling between feedstocks to be examined

COAL/POLYMER COPROCESSING WITH EFFICIENT USE OF HYDROGEN