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Insights into coal structure from degradation with ruthenium tetroxide and tandem mass spectrometry
Authors:KE Singleton  RG Cooks  KV Wood  KT Tse  L Stock
Institution:Department of Chemistry, Purdue University, West Lafayette, IN 47907 U.S.A.;Engine/Fuels Laboratory, Chemistry Building, Purdue University, West Lafayette, IN 47907 U.S.A.;Department of Chemistry, University of Chicago, 5753 S. Ellis Ave., Chicago, IL 60637 U.S.A.
Abstract:The products of ruthenium tetroxid oxidation of coal (Illinois No. 2) at ambient temperature were examined by tandem mass spectrometry using positive and negative chemical ionization. The negative-ion mass spectrum of the coal sample displays seven homologous series of ions. Individual compounds were characterized by recording daughter spectra. In this way, the following types of compounds were identified: aliphatic dicarboxylic acids, aromatic dicarboxylic and tricarboxylic acids, anhydrides of the di- and tri-carboxylic acids, and dianhydrides corresponding to the tetracarboxylic aromatic acids. The positive-ion mass and daughter spectra provided additional confirmation. Two series of ions dominate the positive-ion mass spectrum, those from the aliphatic dicarboxylic acids, and the corresponding anhydrides. The fragmentation behavior of model compounds was examined to confirm these assignments. The carboxylic acids and anhydrides identified suggest the presence of particular structural features in the coal prior to oxidation. These include C2–C6 aliphatic bridges between aromatic units, fused ring aromatic structures, tetralin and indan structures.
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