Influence of phosphonation and phosphation on surface acid–base and morphological properties of CaO as investigated by in situ FTIR spectroscopy and electron microscopy

Pure, phosphated, and phosphonated CaO samples were prepared and characterized by X-ray powder diffractometry, FTIR spectroscopy, scanning electron microscopy, and energy-dispersive X-ray microprobing. Surface acid–base properties were probed by in situ FTIR spectroscopy of adsorbed CO (at 85 K), CDCl3 (at RT), CO2 (at RT), and methyl butynol decomposition reactions (at 473 K). Results obtained have shown phosphate and, to a larger extent, phosphonate additives to enhance the strength of Lewis acid sites exposed on CaO surfaces, at the expense of the Lewis base site strength. The phosphonation has been found, moreover, to make CaO particles grow in a preferential direction and be less susceptible to rehydration. These findings may establish surface chemical attributes for the application of the methylene bisphosphonate (MBP) class of drugs to hamper acid-induced resorption of bone materials (osteoporosis).

Phosphate and, to a larger extent, phosphonate additives enhance the strength of Lewis acid sites exposed on CaO surfaces, at the expense of the Lewis base site strength. Moreover, the phosphonation renders CaO particles less susceptible to rehydration and causes them to grow in a preferential direction.Figure optionsDownload high-quality image (15 K)Download as PowerPoint slide