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Evaluation of acidity of strong acid catalysts. 2. The strength of boron trifluoride-water systems

Journal Article · · Journal of Catalysis; (United States)
OSTI ID:7079987
;  [1]
  1. Univ. of Pittsburgh, PA (United States)
The method of determining a thermodynamic acidity function from the chemical shift changes of {sup 13}C signals of unsaturated ketones at infinite dilution in the investigated acid established by the authors was applied to the system boron trifluoride-water (III) ranging from the monohydrate (BF{sub 3} {center dot} H{sub 2}O) to the trihydrate (BF{sub 3} {center dot} 3H{sub 2}O). The indicators used were mesityl oxide and 4-hexen-3-one. It was found that III is significantly stronger than indicated by earlier measurements conducted by the classical Hammett method based on UV-visible spectroscopy. The mixtures with about 1.25 mol of water per mol of BF{sub 3} or less are stronger than pure sulfuric acid and are therefore superacidic. The stronger acidity of III can be understood because boron trifluoride is a much stronger Lewis acid than sulfur trioxide: therefore the complex with a hydroxyl anion of the former (hydroxytrifluoroborate anion) should have a lower affinity for a hydron than the corresponding complex of sulfuric anhydride (bisulfate anion). Preliminary experiments indicate that the {sup 13}C NMR method can be applied successfully to working catalysts based on III, which are colored and contain dissolved organic materials.
OSTI ID:
7079987
Journal Information:
Journal of Catalysis; (United States), Journal Name: Journal of Catalysis; (United States) Vol. 134:1; ISSN 0021-9517; ISSN JCTLA
Country of Publication:
United States
Language:
English