Aqueous Organic Chemistry. 8. Reactivity of Biaryls

Michael Siskin, David T. Ferrughelli, Alan R. Katritzky, József Rábai

Research output: Contribution to journalArticle

7 Citations (Scopus)

Abstract

Biphenyl, or more accurately biaryl, linkages represent the most refractory cross-links in fossil fuel resources. They are essentially unreactive thermally and in supercritical water at 460 °C. Many biaryls do, however, undergo bond cleavage and heteroatom removal under reducing conditions in supercritical water. 2-Arylpyridines, -quinolines, and -indoles are most reactive in 15% aqueous formic acid whereas the corresponding 2-arylthiophene and -benzothiophene derivatives are more reactive in 15% aqueous sodium formate. Major hydrocarbon products are benzene and naphthalene and their C1-C4 alkylated derivatives. In most cases where conversion is not quantitative after 1 h at 460 °C, the product slate consists of hydrogenated and cleaved products which, given more reaction time, are on the pathway toward complete heteroatom removal.

Original languageEnglish
Pages (from-to)331-343
Number of pages13
JournalEnergy and Fuels
Volume9
Issue number2
DOIs
Publication statusPublished - Mar 1995

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ASJC Scopus subject areas

  • Chemical Engineering(all)
  • Fuel Technology
  • Energy Engineering and Power Technology

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