A comparative study of surface acidity in the amorphous, high surface area solids, aluminium fluoride, magnesium fluoride and magnesium fluoride containing iron(III) or aluminium(III) fluorides

The behaviour of the sol–gel prepared, amorphous solids, high surface area (HS) aluminium fluoride and magnesium fluoride in promoting room temperature dehydrochlorination of tert-butyl chloride (ButCl), in their catalytic activity for the dismutation of chlorodifluoromethane and in the temperature programmed desorption of ammonia is similar, indicating that, unexpectedly, both solids exhibit significant surface Lewis acidity. Using a similar approach, it has been demonstrated that surface Lewis acidity in HS-MgF2 is enhanced by the incorporation of amorphous iron(III) fluoride and probably also by amorphous aluminium(III) fluoride. A second, unexpected feature is the substantial retention of anhydrous hydrogen chloride by all the solids, which is observed by the use of chlorine-36 labelling, when they are exposed at room temperature either to ButCl or to HCl directly. The detailed behaviour of H36Cl towards HS-AlF3 depends on the fluorinating agent, dichlorodifluoromethane or anhydrous hydrogen fluoride, which is used in the second stage of HS-AlF3 synthesis. This observation and the pattern of the results obtained overall lead to the proposal that strongly adsorbed HCl behaves as an unconventional Lewis base towards these solids.

Dehydrochlorination of ButCl, studied by FTIR and [36Cl]-labelling, NH3 TPD and catalytic dismutation of CHClF2 are used to compare Lewis acidity at HS-AlF3 and HS-MgF2 surfaces.Figure optionsDownload as PowerPoint slide