Mechanisms of formation and reactivity of imogolite types material

Reactivity of nanopar8cles represents a central issue for many laboratories around the world. Among many supported efforts the control of the morphology of nanopar8cles is mo8vated by the fact that morphology strongly influence the proper8es of the final products. Among the vast family of available nanopar8cles, imogolite is a clay nanotube for which perfect control of the diameter is possible. Imogolites were first observed in volcanic soils[1]. They are natural aluminosilicate nanotubes having the general formula (OH)3Al2O3SiOH with a 2 nm external diameter and up to micrometers in length. The impressive monodispersity in imogolite nanotube diameter has mo8vated research on their forma8on mechanism. Synthesis protocols to produce imogolite were quickly developed. Farmer et al. were the first to obtain synthe8c imogolite using low concentra8ons of AlCl3 and SiO 2 monomers as star8ng materials (millimolar concentra8ons of the reagents) [2]. However, the produc8on of large amount of imogolite or imogolite type materials remained challenging for long 8me. We will present our most recent results concerning the possibility to produce imogolite type materials from highly concentrated stock solu8ons. We will also detail the possibility to form double wall Al- Ge nanotubes and the different stages of their forma8on [3-7]. We will then detail the surface reac8vity of these nanotubes toward metals at he lab scale as well as in natural soil. (Résumé d'auteur