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| - Hydrogen Transfer in the Formation and Destruction of Retrograde Products in CoalConversion
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| - The conversion of coals to volatiles or liquids during pyrolysis and liquefaction is notoriously limited by theformation of retrograde products. Analysis of literature data for coals with grafted structures and for polymericcoal models demonstrates that the formation of volatile products from these materials does not correlateprimarily with the weakness of the original bonding but correlates with the facility for retrogressive reaction.This analysis suggests further that simple recombination of resonance-stabilized radicals does not tend toyield true retrograde products, except in the case of aryloxy radicals. For pure hydrocarbon structural elements,radical addition to aromatic systems appears to be a key class of retrograde reactions, where the key factoris the kinetics of radical or H-atom loss from a cyclohexadienyl intermediate. We have used a mechanisticnumerical model with a detailed set of radical reactions and thermochemically based kinetic parametersoperating on a limited set of hydrocarbon structures to delineate important factors in mitigating retrogradeprocesses. The modeling results show (1) how the “better” radical scavengers may reduce retrograde reactionat short reaction times but actually tend to increase it at longer times; (2) that the beneficial effects of H2pressure at short reaction times are not primarily due to lowering of harmful radical concentrations byscavenging, nor to the maintenance of donor content; (3) that the benefit is due to the small population offree H-atoms thus produced, which are very active in causing increased scission of strong bonds; and (4) thatunder some conditions retrograde products are actually generated faster with added H2, but at longer reactiontimes and higher temperatures this temporary disadvantage of H2 is overcome by increased hydrogenolysisof those earlier-produced retrograde products. Thus, not only the cleavage of critical bonds in the originalcoal structures but also the net prevention of retrogression may be due to the H-transfer-induced cleavage ofstrong bonds.
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